Abstract: An apparatus for measuring distensibility of a vessel, lumen or sphincter includes a balloon catheter having a balloon located adjacent a distal end of a catheter for inserting in, for example, the sphincter, the distensibility of which is to be determined. The balloon is inflated to respective first and second pressures to distend the sphincter to respective first and second transverse cross-sectional areas which are measured. The first and second pressures are selected so that the relationship between the pressure and the cross-sectional area of the sphincter is linear. The distensibility of the sphincter is determined as a distensibility index, which is the value of c from the equation of a line y=mx+c containing the values of the first and second pressures and areas, where x represents pressure and y represents area.

Abstract: A medical system provides navigation assistance to a surgeon for navigating a flexible medical device through linked passages of an anatomical structure to a target area. For tracking, navigation, and other purposes, information of extrema is determined during expansion and contraction cycles of an object by receiving time sampled information from sensors distributed along a length of a flexible device so as to indicate the shape of the device over time while the device extends through a lumen of the object so as to conform to and resemble the shape of the lumen, displacements over time of a selected point at a selected insertion length of the flexible device into the lumen of the object relative to a reference point are determined, extrema time points are determined by identifying sign changes of the slope of the determined displacements over time, and extrema types are determined using extrema type characteristics.

Abstract: Disclosed herein is a method and apparatus for swallowing impairment detection, whereby a candidate executes one or more swallowing events and dual axis accelerometry data is acquired representative thereof. Upon feature extraction and classification, vibrational data acquired in respect of each swallowing event is classified as indicative of one of normal or possibly impaired swallowing. Computer-readable media comprising statements and instructions for implementation by a processing device are also described in facilitating swallowing impairment detection respective to candidate swallowing events.

Abstract: A bolus for insertion in a body fluid includes a housing, a chamber in the housing admitting body fluid therein, and a transducer in the housing providing a signal through the body fluid for measuring the pH level and/or temperature of the body fluid. The transducer also generates a signal in response to vibrations to detecting one or more additional physiological parameters.

Abstract: A system (1) and a device (3) is used in a fundoplication procedure in order to avoid over-tightening of the fundus of the stomach when the fundus is being wrapped around the esophagus (7) adjacent the lower oesophageal sphincter (5). The device (3) comprises a catheter (8) having a primary balloon (12) located at a distal end (9) thereof which is inflatable with a saline solution by a primary pump (26). A pair of spaced apart primary stimulating electrodes (32) on the catheter (8) within the primary balloon (12) receive a stimulating current signal from a constant current signal generator (40) under the control of a microprocessor (43), which reads voltage signals from spaced apart primary receiving electrodes (35) on the catheter (8) in the balloon (12).

Abstract: The proposed invention is a method and system for the segmentation of dual-axis accelerometry signals for the purpose of identifying problematic swallowing events. The method and system employ a sensor, a data collection means including an algorithm for analysis of the data. The proposed invention considers the stochastic properties of swallowing signals in both directions, A•P and S-I to extract events associated with swallowing. A segmentation algorithm may be applied to the signals to establish the time duration of swallows and swallows may be classified with respect to gender, body mass index, age or types of swallow.

Abstract: Systems and methods for effecting bariatric procedures are disclosed. Each system includes an instrument, a control valve and, optionally, a suction controller. The instrument is in the form of an elongated, flexible sizing tube having a distal end portion including a plurality of apertures. The control valve enables suction to be applied to the patient's stomach via the apertures to drain gastric fluids and to bring adjacent portions of the patient's stomach into engagement the sizing tube to provide a visually perceptible delineation line along which a portion of the stomach may be resected, sealed and tested.

Abstract: Systems and methods for effecting bariatric procedures are disclosed. Each system includes an instrument, a control valve and, optionally, a suction controller. The instrument is in the form of an elongated, flexible sizing tube having a distal end portion including a plurality of apertures. The control valve enables suction to be applied to the patient's stomach via the apertures to drain gastric fluids and to bring adjacent portions of the patient's stomach into engagement with the sizing tube to provide a visually perceptible delineation line along which a portion of the stomach may be resected, sealed and tested.

Abstract: A passive wireless gastroesophageal sensor includes a LC resonance circuit, two or more electrodes and a passive batteryless Radio Frequency Identification (RFID) circuit connected to the LC resonance circuit and the one or more electrodes. The electrodes are configured to measure an impedance within a gastroesophageal tract. The passive batteryless RFID circuit transmits a frequency modulated signal using the LC resonance circuit that varies between a first frequency corresponding to a non-acid reflux condition and a second frequency corresponding to an acid reflux condition based on the measured impedance in response to a signal received from a detector.

Abstract: A method of determining body exit of an ingestible capsule comprising the steps of providing (40) an ingestible capsule (20) having a pressure sensor (23), having (41) a subject ingest the capsule, recording (42a) measurements from the pressure sensor as the capsule passes through at least an end portion of a gastrointestinal tract of the subject, transmitting (44) the measurements to a processor (31) outside of the gastrointestinal tract of the subject, identifying (47) an increasing pressure sequence (65) in the measurements between a selected start time (62) and a transmission end time (63), comparing (48) the sequence to a reference (66), and using the comparison to make a determination (52) regarding the capsule exiting the gastrointestinal tract of the subject. The increasing pressure sequence may be the longest increasing pressure sequence in the measurements. The reference may be a logarithmic regression of the measurements.

Abstract: One or more techniques and/or devices are disclosed for promoting standardization of the dissection of a portion of a patient's stomach, such as during laparoscopic sleeve gastrectomy (LSG), for example. In this way, LSG can be improved at least by allowing a surgeon and/or patient to choose a post surgery stomach size in a quantifiable manner. For example, a patient could discuss various stomach sizing options with their doctor and select the option believed to be most beneficial to the patient. Moreover, one or more techniques and/or devices are disclosed for decreasing tissue trauma while performing surgical stapling, such as during LSG. In this way, surgical procedures that implement stapling can be improved, as reduced tissue trauma generally accelerates healing time, among other things. For example, staples and/or staple cartridges may be designed to reduce pinching or pressure points along a staple line while achieving desired closure and/or hemostasis.

Abstract: A system and method for indicating transferability of a non-dissolvable target in-vivo device through the GI tract are described. The in vivo system includes a dissolvable in-vivo device which has two operational phases; an initial phase in which the device is of initial dimensions and a final phase in which the device is of final dimensions. In the initial phase the device can pass freely through a normally configured body lumen whereas it may not be able to pass freely through an abnormally configured lumen. In the final phase the device can pass freely through a body lumen even if it is abnormally configured.

Abstract: A system for monitoring strain as an indicator of biological conditions, such as spinal fusion, glucose levels, spinal loading, and heart rate. The system includes an inter-digitated capacitor sensor, and RF transmitter, and an associated antenna, all of which are microminiature or microscopic in size and can be implanted in a biological host such as a human or animal. An inductively coupled power supply is also employed to avoid the need for implantation of chemical batteries. Power is provided to the sensor and transmitter, and data is transmitted from the sensor, when an external receiving device, such as a handheld RF ID type receiver, is placed proximate the location of the implanted sensor, transmitter and inductively coupled power supply. The implanted sensor, transmitter and inductively coupled power supply can be left in place permanently or removed when desired.

Abstract: A device and method for mapping, diagnosing and treating disorders or other diseases, disorders or conditions (e.g., bleeding, ischemic or necrotic tissue, and presence of certain chemicals or substances) of the intestinal tract is provided using a capsule passing through the intestinal tract and sensing optical characteristics as the capsule passes through. Further, a capsule tracking system is provided for tracking a capsule's location along the length of an intestinal tract as various treatment and/or sensing modalities are employed. In one variation, an acoustic signal is used to determine the location of the capsule. A map of optical characteristics may be derived from the pass of a capsule to diagnose the disorder or disease. The capsule or subsequently passed capsules may treat, further diagnose or mark the intestinal tract at a determined location along its length.

Abstract: A neonatal feeding tube (10) includes electronics and instrumentation for monitoring a neonate and for provides nourishment to the neonate. The tube (10) includes electrodes (20) for sensing ECG signals of the neonate. Thermistors (22, 24, 28, 30) are placed at various points along the tube (10) to measure the neonate's temperature at those points. Breathing effort is measured by calculating a pressure differential at two pressure ports (32, 34). Pulse and SpO2 are measured at a fiber optic window (35). The electrodes (20), a distal electrode (64) and a light source (66) aid in helping a caregiver position the tip (12) of the tube (10) correctly in the stomach of the neonate.

Abstract: Gastric apparatus is provided, including one or more sensors, adapted to generate respective sensor signals responsive to activity of a gastrointestinal tract of a subject. A control unit is configured with an eating detection threshold selected from the group consisting of: a predetermined threshold, and a threshold determined during a calibration procedure. The control unit is adapted to receive and analyze the sensor signals, and identify an aspect of at least one of the sensor signals indicative of periodic activity of the gastrointestinal tract. The control unit modifies the eating detection threshold responsive to identifying the aspect of the signals that is indicative of the periodic activity, and determines that an eating event has occurred responsive to the modified eating detection threshold and at least one of the analyzed sensor signals. Other embodiments are also described.

Abstract: Configuration technologies for cost-effectively monitoring indicia of regimen compliance or noncompliance in response to one or more indications of symptoms or actions or other data on data-bearing media or in wireless transmissions, such as implementing techniques for providing or preventing access or otherwise acting on or communicating incremental or definitive indicia of compliance or noncompliance.

Abstract: The present disclosure is directed to apparatuses and methods for diagnosing a swallowing dysfunction. The apparatuses may include a multi-parametric dysphagia analysis system in a plastic foil. The analysis systems may be smart sensing systems that are flexible, lightweight, and based on substrates having low-cost printed electronics technologies thereon. The methods may include measurement and classification of non-invasive parameters that may be indicative of a swallowing dysfunction or the probability of same. In a general embodiment, the methods include placing a sensor on a patient for measurement of at least one parameter associated with the patient's swallowing profile. The measured parameter is then analyzed and compared with several known normal and dysphagic swallowing profiles to provide an indication of the probability of an underlying swallowing dysfunction.

Abstract: An abdomen width determiner determines an abdomen width of a subject. A shape index calculator calculates a shape index corresponding to a cross-sectional shape of an abdomen of the subject. An obesity evaluator evaluates whether an obesity degree of the subject is high or low. An obesity index calculator calculates an obesity index corresponding to the abdomen width using a first equation if the obesity evaluator evaluates that the obesity degree is low, and calculates an obesity index corresponding to the abdomen width and the shape index using a second equation different from the first equation if the obesity evaluator evaluates that the obesity degree is high.

Abstract: The present invention provides compositions and methods useful in the diagnosis and management of Gastroesophageal Reflux. Specifically, the inventions provide a device and methods of using the device for accurately, quantitatively, and non-invasively diagnosing Gastroesophageal reflux disease (GERD) in both patients at risk for GERD and patients demonstrating reflux-like symptoms. In particular, the inventions relate to detecting and analyzing upward esophageal movements in patients, such as human infants, children, and adults.

Abstract: A trocar device and measurement assembly, includes a trocar having a sharply pointed shaft and a handle. An elongated sheath receives the shaft of the trocar therein, wherein the elongated sheath includes a plurality of measuring indicia thereon for measuring a length of a tracheoesophageal puncture formed by the trocar. A method of measuring the tracheoesophageal puncture is provided by inserting the elongated sheath into the puncture while observing the measuring indicia on the sheath to determine a length of the puncture.

Abstract: An apparatus for determining an optimal amount of tissue compression for applying a surgical element to tissue is disclosed. The apparatus includes a device for compressing tissue which supports a measuring device adapted to detect a tissue parameter upon the compression of tissue. The measuring device communicates with an indicator. Upon compressing tissue, when the measuring device determines that the compressed tissue parameter reaches a predetermined threshold, the measuring device sends a signal to the indicator such that the indicator provides an indication to a surgeon that the threshold has been reached. The measuring device may include a load cell and the tissue parameter may be a viscoelastic reactive force of the tissue per unit time.

Abstract: An in-vivo examining device, system and method for identifying the presence of strictures in the small bowel are provided. The in-vivo examining device includes a monitoring mechanism that becomes deactivated when exposed to in-vivo substances native to the small bowel or the colon, and a degradable device body that includes at least a first body portion which degrades at a slow rate when exposed to in-vivo substances native to the small bowel and at a fast rate when exposed to in-vivo substances native to the colon. The degradation of the degradable device body exposes the monitoring mechanism to substances native to the small bowel or the colon and thus indicates whether the examining device has safely passed through the small bowel or whether it is retained in the small bowel due to strictures in the small bowel.

Abstract: A method and apparatus for determining the volume of a pouch formed in a stomach during bariatric surgery comprises a balloon catheter having an inflatable balloon located at a distal end of a catheter for locating in the stomach. A pair of spaced apart stimulating electrodes are located on the catheter within the balloon and a plurality of spaced apart sensing electrodes are located on the catheter between the stimulating electrodes. The balloon in the stomach is inflated by a saline solution to define the interior of the pouch. By applying a constant current signal to the stimulating electrodes, the volume of the pouch is determined from signals read from the sensing electrodes.

Abstract: A device and method for mapping, diagnosing and treating the intestinal tract is provided using a capsule passing through the intestinal tract. Further, a capsule tracking system is provided for tracking a capsule's location along the length of an intestinal tract as various treatment and/or sensing modalities are employed. In one variation, an acoustic signal is used to determine the location of the capsule. A map of sensed information may be derived from the pass of a capsule. Capsules may be subsequently passed through to treat the intestinal tract at a determined location along its length. One variation uses an electrical stimulation capsule to treat and/or diagnose a condition in the intestinal tract.

Abstract: The present invention provides an apparatus for distributed pressure sensing. The apparatus comprises a series of Bragg gratings, a light guide incorporating the series of Bragg gratings and a plurality of moveable wall portions. The moveable wall portions are coupled to respective Bragg gratings so that the movement of one of the moveable wall portion causes a force on the respective Bragg grating resulting in a change in strain of the respective Bragg grating. The apparatus also comprises at least one rigid member that is attached at attachment regions between which a sensing region of at least one Bragg grating is defined. The rigid member is arranged so that a strain in the sensing region is not directly influenced by a change in strain of the light guide outside the sensing region.

Abstract: A system for measuring the size of a gastric lumen includes a gastric banding device, an antenna positioned outside of the patient's body, and a receiver in operative communication with the antenna. The banding device comprises two orthogonal ultrasonic transceiver modules, a microprocessor, and a transmitter in electrical communication with the microprocessor. The microprocessor is in operative communication with each of the two transceiver modules. The transmitter transmits signals to a receiver positioned outside of a patient's body. Another system for measuring the size of a gastric lumen includes a gastric banding device having a first coiled conductor. The system further comprises a circuit external to the banding device, the circuit comprising a second coiled conductor. The circuit further comprises a tunable frequency generator and a spectrum analyzer, the circuit being tunable to allow a resonant frequency.

Abstract: Devices and systems to size a luminal organ. At least some embodiments include a catheter comprising an outer elongate tube, an inner elongate tube disposed within the outer elongate tube, a proximal balloon attached to the outer elongate tube, a distal balloon having a first end attached to the outer elongate tube and a second end attached to the inner elongate tube, electrodes positioned on the outer elongate tube, and a pressure transducer positioned on the outer elongate tube.

Abstract: A probe system includes a finger-mountable housing having a distal end and a proximal receptacle end. The proximal receptacle end defines an opening to receive a finger. The probe system also includes a probe assembly disposed on or within the finger-mountable housing and having at least a first sensor. The first sensor is positioned to measure a physical characteristic of a first tissue when the finger-mountable housing and probe assembly are inserted in a rectum of the patient.

Abstract: A lumen passability checking device includes: an expandable and shrinkable outer casing that contains a predetermined fluid, is expanded by a pressure of the contained fluid, and forms an external diameter substantially equal to that of a capsule medical device to be inserted into a body of a subject; and a shape manipulating unit that flows out the fluid contained in the outer casing to shrink-deform the outer casing. The outer casing is shrink-deformed by flowing out the fluid, while maintaining a state of being integrated with the shape manipulating unit.

Abstract: An intestinal peristalsis detecting device comprises a radio frequency (RF) signal generator, an antenna, and a mixer. After the RF signal generator sends a pulse signal, the antenna receives the pulse signal and emits a pulse electromagnetic wave to an organism. Thereafter, the antenna receives a response pulse electromagnetic wave reflected from the organism to generate a response pulse signal. The mixer couples with the RF signal generator and the antenna to mix the pulse signal and the response pulse signal.

Abstract: An esophageal device is used to recognize, diagnose, characterize, or relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality. In one implementation, the esophageal device measures a UES response to esophageal fluid infusion to detect or characterize an abnormality or defective UES anatomy, physiology, or functionality. An Upper Esophageal Sphincter compression device is used to increase intra-luminal pressure within the Upper Esophageal Sphincter of a patient in order relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality.

Abstract: An oral device for use with a person in which at least one non-toxic gas pulse is delivered to a predetermined location in the mouth via a device conduit. The oral device may be provided as a kit with at least one device for measuring the subject's responses and representing them as feedback to the subject/clinician. A method of creating a gas bolus pulse train, delivering it to a predetermined mouth area, and monitoring the subject's responses to it, is also shown. The oral device and method may be used as a diagnostic tool, or a therapeutic tool, in swallowing or speech rehabilitation of children and adults who have swallowing, speech, salivary, and/or oral sensorimotor impairments.

Abstract: Described herein is an apparatus that includes an endotracheal tube or airway device having a proximal end and a distal end and an occlusion cuff. The occlusion cuff includes a sensor for helping determine proper endotracheal or airway device placement.

Abstract: A device and method for mapping, diagnosing and treating disorders or other diseases, disorders or conditions (e.g., bleeding, ischemic or necrotic tissue, and presence of certain chemicals or substances) of the intestinal tract is provided using a capsule passing through the intestinal tract and sensing optical characteristics as the capsule passes through. Further, a capsule tracking system is provided for tracking a capsule's location along the length of an intestinal tract as various treatment and/or sensing modalities are employed. In one variation, an acoustic signal is used to determine the location of the capsule. A map of optical characteristics may be derived from the pass of a capsule to diagnose the disorder or disease. The capsule or subsequently passed capsules may treat, further diagnose or mark the intestinal tract at a determined location along its length.

Abstract: The proposed invention is a method and system for the segmentation of dual-axis accelerometry signals for the purpose of identifying problematic swallowing events. The method and system employ a sensor, a data collection means including an algorithm for analysis of the data. The proposed invention considers the stochastic properties of swallowing signals in both directions, A-P and S-I to extract events associated with swallowing. A segmentation algorithm may be applied to the signals to establish the time duration of swallows and swallows may be classified with respect to gender, body mass index, age or types of swallow.

Abstract: Methods to size a gastric pouch. In at least one embodiment for measuring the size of a gastric pouch of the present disclosure, the method comprises the steps of introducing a catheter into an esophagus, the catheter comprising an outer elongate tube, an inner elongate tube disposed within the outer elongate tube, a proximal balloon attached to the outer elongate tube, a distal balloon having a first end attached to the outer elongate tube and a second end attached to the inner elongate tube, at least two detection electrodes positioned on the outer elongate tube between at least two excitation electrodes, and a pressure transducer positioned on the outer elongate tube, locating the gastroesophageal junction using the proximal balloon, adjusting the distal balloon axially to a desired balloon length, injecting a fluid into the distal balloon to extend the distal balloon circumferentially, and determining a size variable of the gastric pouch.

Abstract: Methods for assessing an overall digestive health of a patient are provided, which include administering a breath test that uses a label incorporated into proteins, carbohydrates, and lipids and further incorporating the labeled material into a meal which, when cooked, facilitates the binding of the label material to the solid phase matrix of the meal. Methods for assessing digestive functions of a patient are also provided, which includes concurrently administering a breath test and a scintigraphy test that measure gastric emptying in a stomach.

Abstract: A medical system provides navigation assistance to a surgeon for navigating a flexible medical device through linked passages of an anatomical structure to a target area. For tracking, navigation, and other purposes, information of extrema is determined during expansion and contraction cycles of an object by receiving time sampled information from sensors distributed along a length of a flexible device so as to indicate the shape of the device over time while the device extends through a lumen of the object so as to conform to and resemble the shape of the lumen, displacements over time of a selected point at a selected insertion length of the flexible device into the lumen of the object relative to a reference point are determined, extrema time points are determined by identifying sign changes of the slope of the determined displacements over time, and extrema types are determined using extrema type characteristics.

Abstract: A diagnostic system for display of physiological data in a format useful for identifying or diagnosing physiological conditions. The system registers visual representations of different types of physiological data to aid in an understanding of bodily processes. In addition to registering the data, the system may display different types of physiological data with different visual characteristics. Further, the transparency of the visual representations of the different datasets may be controlled to enhance the understandability of displayed information. The system, for example, can be used with data representative of pressure and impedance within a patient's gastrointestinal tract to provide greater understanding of physiological processes during a swallow.

Abstract: Systems and methods for treating gastroesophageal reflux disease (GERD) includes minimally invasively implanting a stimulating device in a patient's esophagus in the region proximate the lower esophageal sphincter (LES). The patient is provided with a questionnaire related to his disease via an online service. The questionnaire is accessed on a mobile device, such as a cell phone, or on a computer with network access. The data from the sensors and the answers from the questionnaire are analyzed together by a health care provider using the online service. The data and answers are used to program the stimulating device, via the mobile device or computer, to optimize treatment.

Abstract: Disclosed is a swallowing test apparatus including a laryngeal part displacement detection apparatus for detecting a distance of two positions located laterally at a laryngeal part of a subject, a swallowing sound detection apparatus for detecting a swallowing sound of the patient during swallowing, a display, a processing apparatus for displaying a waveform representing the distance of the two positions at the laryngeal part generated based on a signal obtained from the laryngeal part displacement detection apparatus, and a waveform representing the swallowing sound generated based on a signal obtained from the swallowing sound detection apparatus on the display.

Abstract: The proposed invention is a method and system for the segmentation of dual-axis accelerometry signals for the purposed of identifying problematic swallowing events. The method and system employ a sensor, a data collection means including an algorithm for the analysis of the data. The proposed invention considers the stochastic properties of swallowing signals in both directions, A-P and S-I to extract events associated with swallowing. A segmentation algorithm may be applied to the signals to establish the time duration of swallows and swallows may be classified with respect to gender, body mass index, age or types of swallow.

Abstract: Gastric emptying classification systems, displays, methods for classifying gastric emptying data, methods for treating patients, and methods for developing gastric emptying classification systems are disclosed.

Abstract: An esophageal mapping catheter enables a physician to map the location of the esophagus so as to avoid damaging the esophagus during radio frequency (RF) ablation procedures. Information from the esophageal mapping catheter is communicated to a patient information unit, communications unit and/or electroanatomic mapping system. The electroanatomic mapping system uses the information from the esophageal mapping catheter to develop a three-dimensional map of the esophagus and to monitor the temperature within the esophagus in order to prevent the creation of esophageal fistula.

Abstract: Anastomosis leak testers for testing for leaks in gastrointestinal anastomoses in patients include an inflation pump and a conduit part. The inflation pump has a compressible portion and a mechanism for providing a uni-directional flow of air through the inflation pump upon intermittent compressing thereof. Conduit parts have an interior space, a portion to be inserted into an anus of a patient or arm to be mated to a gastric tube, rectal tube or endoscope, a pressure relief valve and an indicator pin, and a rearward arm connected to the inflation pump. Upon actuation of the inflation pump, air flows through the inflation pump and through the conduit part into the patient's bowel. When the air pressure in the bowel exceeds a specified pressure, air is released through the pressure relief valve and ejects the indicator pin, which alerts the surgeon that the desired rectal pressure has been reached.

Abstract: A medical device implanted within a lumen of a patient, such as the esophagus, stomach, or another portion of the gastrointestinal tract, includes a device housing and a lead that extends from the device housing. An anchor member is located at a distal portion of the lead, and the lead includes one or more electrodes located between the device housing and the anchor member. A delivery system for implanting the medical device within the lumen includes an elongated delivery device and a needle. The needle includes a bore to receive the anchor member of the medical device. The delivery system inserts the anchor member through a passageway from the lumen, through the tissue, and back into the lumen.

Abstract: A method for measuring physiological parameters uses statistical properties, spectrum analysis and feedback mechanisms to remove the signal noise generated by human body movement from a detected physiological signal.

Abstract: An image display apparatus includes a display unit that displays images contained in a plurality of image groups inside a subject picked up by a plurality of imaging devices, and a control unit that extracts a related image related to a currently displayed image currently displayed in the display unit from the plurality of image groups to make the display unit display the related image extracted.

Abstract: A system for measuring the size of a gastric lumen includes a gastric banding device, an antenna positioned outside of the patient's body, and a receiver in operative communication with the antenna. The banding device comprises two orthogonal ultrasonic transceiver modules, a microprocessor, and a transmitter in electrical communication with the microprocessor. The microprocessor is in operative communication with each of the two transceiver modules. The transmitter transmits signals to a receiver positioned outside of a patient's body. Another system for measuring the size of a gastric lumen includes a gastric banding device having a first coiled conductor. The system further comprises a circuit external to the banding device, the circuit comprising a second coiled conductor. The circuit further comprises a tunable frequency generator and a spectrum analyzer, the circuit being tunable to allow a resonant frequency.