Abstract: A method for treating a tumor, comprising identifying a tumor as a squamous cell carcinoma tumor and implanting in the tumor identified as a squamous cell carcinoma tumor at least one diffusing alpha-emitter radiation therapy (DaRT) source (21) with a suitable radon release rate and for a given duration, such that the source (21) provides during the given duration a cumulated activity of released radon between 3.7 Mega becquerel (MBq) hour and 8.6 MBq hour, per centimeter length.

Abstract: The present invention discloses a motion sickness prevention wristband and a control method thereof, wherein the motion sickness prevention wristband comprises wristband body, and further comprises microcontroller unit MCU, pressure sensor, electrode assembly, and air bag control assembly; pressure sensor, electrode assembly, and air bag control assembly are electrically connected to the MCU, and air bag control assembly is resisted against electrode assembly; pressure sensor, for obtaining contact pressure value between electrode assembly and the surface of the human skin; the MCU, for determining air pressure control data; and air bag control assembly, control air pressure change to enable the MCU to apply electrical stimulation to electrode assembly after the air pressure change.

Abstract: An ocular positioning system for use with a magnetic treatment apparatus for treating an eye of a subject is provided, where the magnetic treatment apparatus includes a magnetic coil for generating a magnetic field and an electric field. The ocular positioning system includes a housing having a proximal end and a distal end, wherein the magnetic coil is disposed in the housing near the proximal end. A positioning member is at least partially attached to the housing proximal end, the positioning member including a base and an eyecup coupled thereon, where the eyecup is configured to receive an orbital region of the subject. At least one sensor is connected to the housing and in electrical communication with the magnetic coil, wherein when the at least one sensor detects the positioning member then the magnetic coil is capable of being activated for treatment.

Abstract: The present disclosure pertains to facilitating sleep improvement for a user. In a non-limiting embodiment, user data associated with a sleep session of a user is received from one or more sensors. Based on the user data, one or more sleep metrics associated with the sleep session are generated. One or more reference sleep metrics are determined based on prior user data obtained from one or more prior sleep sessions. One or more immediate values related to the sleep session is/are determined based on a comparison of the sleep metrics with the reference sleep metrics. A sleep session score value is generated based on the immediate values, and the sleep session score value and the sleep metrics are caused to be presented on via an output device.

Abstract: Wearable devices that provide tactile, visual stimulation, and movement/manipulation for a user are described. The devices can include a spinner that rotates with respect to a base. The spinner can be spun by the user to produce visual stimulation that the user may find pleasing and soothing, and which may provide therapeutic effects. The spinner may also include tactile features, such as a series of protrusions and recesses, that the user can touch or rub to create a tactile sensation, which may also help the user to relieve and/or regulate stress. The spinner also allows the user to manipulate the spinner with fingers in small repetitive movements that may reduce restlessness. The devices may be sized and shaped such that the user may uninterruptedly perform everyday tasks and discretely wear and use the devices in certain social environments such as the classroom.

Abstract: A minimally invasive medical instrument comprises an elongate flexible body comprising a proximal portion, a distal portion, a transition portion between the proximal portion and the distal portion, and an inner sheath extending at least within the proximal portion. The inner sheath comprises a plurality of conduits extending through a wall of the inner sheath. A distal end of each conduit terminates at the transition portion. The flexible body further comprises a steerable tube extending within the distal portion. The steerable tube comprises a plurality of grooves in a wall of the steerable tube. The medical instrument further comprises at least one tendon extending from the proximal portion into the distal portion of the flexible body. In the proximal portion, the tendon extends through at least one conduit of the plurality of conduits. In the distal portion, the tendon extends within at least one groove of the plurality of grooves.

Abstract: A system and method for controlling the speed of operation of sexual stimulation devices from videos of sexual activity using a less computationally intensive method of estimating movement speed from a video. In an embodiment, the system and method involve estimating movement in a video using pixel-by-pixel color change over time, calculating a rate of color change in the video, estimating a speed of movement in the video from the rate of color change, and applying an algorithm to convert the estimated speed of movement in the video to a speed of operation of a sexual stimulation device.

Abstract: Certain configurations are described of devices that can receive and retain a radiation measuring device during administration of a nuclear medication. In some instances, the radiation measuring device can measure radiation levels being delivered through an intravenous line positioned within the device and connected to a patient. Methods and systems using the devices are also described.

Abstract: Neural stimulator systems with an external magnetic coil to produce changing magnetic fields is applied outside the body, in conjunction with one or more tiny injectable objects that concentrates the induced electric field to a highly-targeted location. These systems include a driver circuit for the magnetic coil that allows for high voltage and fast pulses in the coil, while requiring low-voltage power supply that may be powered by a wearable or portable external device, along with the coil and driver circuit.

Abstract: Methods and devices for reducing inflammation, reducing pro-inflammatory cytokines molecules and increasing anti-inflammatory signaling molecules in a mammal is provided. In at least one embodiment, a device comprising, a power supply; an amplifier; an antenna and a waveform generator is provided and the one or more signals have an aperiodic continuous waveform function or an aperiodic pulse train that reduce inflammation, reduce pro-inflammatory cytokines molecules and/or increases anti-inflammatory signaling molecules in a mammal.

Abstract: A diagnostic hub located in a toilet receives a wireless signal from a mobile device of a user and determines that the user is proximate to the toilet based on the wireless signal. An identification of the user is determined based on the wireless signal. A geolocation of the diagnostic hub is determined. Sensor data generated by biometric sensors and environmental sensors is received. The diagnostic intakes a mixture of water and urine from the toilet into an intake chamber of the diagnostic hub through an inlet line or one or more openings in a housing of the diagnostic hub. A lab-on-a-chip of the diagnostic hub executes a biochemical assay on a fluid volume of the mixture using a reagent. Substance levels present in the urine are determined based on the biochemical assay. Results based on the substance levels are determined, indicating a diagnosis of one or more diseases or medical conditions.

Abstract: A method used for planning radiation treatment accessing information that includes calculated doses and calculated dose rates for sub-volumes in a treatment target, and also accessing information that includes values of a measure of the sub-volumes as a function of the calculated doses and the calculated dose rates. A graphical user interface includes a rendering that is based on the calculated doses, the calculated doses rates, and the values of the measure.

Abstract: An intraosseous access system can include a needle that defines a lumen and a longitudinal axis about which the needle can be rotated during an insertion event. The needle can include a proximal end that remains at an exterior of a patient during use, a distal end that can be inserted through the skin of the patient into contact with a bone of the patient, and a distal tip at a distalmost point of the distal end of the needle that is positioned at the longitudinal axis of the needle. The system can further include an obturator sized to be received within the lumen of the needle that can inhibit material from entering the needle as the system is inserted into the bone.

Abstract: An adult toy is configured to communicate with a user device of a human user. Receipt of a plurality of input parameters is accumulated via the user device. In response to the accumulation satisfying a preset condition, the accumulation is stopped and a control signal is sent to actuate the adult toy to perform a series of predefined acts. The series of predefined acts are used to sexually stimulate the human user. The control signal includes one or more control sub-patterns, each of the one or more control sub-patterns being configured by each of the plurality of input parameters.

Abstract: To provide a surgical clip capable of being held by, in particular, a robot arm or other device, thus promoting automation of a procedure. A surgical clip to pull an organ or other body tissue so as to provide an area necessary for an operation includes: a pair of upper and lower holders to hold the organ or other body tissue therebetween; a grip to open and close the holders; an urger to constantly urge the holders in a holding direction; and an engagement portion provided on the grip. The engagement portion comes into engagement with a hole defined in a functional part provided on a medical device that includes any one of a robot, forceps, and an applier. The functional part is configured to open and close so as to perform a holding, incising, or other operation.

Abstract: The invention relates to a tissue receiving bag for use in surgery, especially laparoscopic surgery, wherein the bag comprises at least one tissue receiving opening for receiving tissue and/or an instrument opening, especially a morcellator opening, wherein the bag comprises at least one further opening into the bag, wherein a flexible tube extends from said further opening having a free end comprising an insertion opening for inserting an instrument into the bag, wherein the bag preferably is inflatable.

Abstract: A brachytherapy device including a base adapted for being at least partially introduced into a body of a subject and a plurality of radionuclide atoms of a first alpha-emitting isotope, coupled to the base in a manner that not more than 15% of the radionuclide atoms leave the base in 24 hours, in methods other than radioactive decay. When installed in a human subject, the brachytherapy device emits radionuclide atoms of the first alpha-emitting isotope at a rate of at least 0.1% of the number of radionuclide atoms of the first alpha-emitting isotope coupled to the base, per 24 hours.

Abstract: A method for treating a tumor, comprising identifying a tumor as a prostate cancer tumor and implanting in the tumor identified as a prostate cancer tumor, at least one diffusing alpha-emitter radiation therapy (DaRT) source with a suitable radon release rate and for a given duration, such that the source provides during the given duration a cumulated activity of released radon between 7 Mega becquerel (MBq) hour and 14.7 MBq hour, per centimeter length.

Abstract: This present invention is a novel method and wearable device for stimulating positive DNA gene expression and mitigating negative DNA gene expression in order to improve health and wellness. The invention's unique characteristics include the application of multiple modalities, their unique configuration for safe, low-power application, the wearable device's unique arrangement in a flat, flexible configuration for elastic contouring with comfort required for an extended period of wearing, and the ability to optimize and personalize the parameters and mixing among such modalities. The invention further combines biometric feedback data with Artificial Intelligence analytic capabilities, to facilitate the identification and characterization of DNA resonant frequencies, and associated “stimulus-response” modeling associated with such biological interactions.

Abstract: An interactive sex toy with sensory feedback is described herein. The sex toy may include a main body upper shell, a main body lower shell, and several trigger buttons, wherein the four trigger buttons are encased in the main body shell. Each of the four trigger buttons may include a mechanical spring and a conductive foam plastic. A motor maybe activated on a condition that at least one of the four trigger buttons is depressed. A pressure level may increase when an additional trigger button is depressed. A method for using an interactive sex toy with sensory feedback may include receiving physical pressure readings from an interactive sex toy with sensory feedback at a first device, converting the physical pressure readings to pressure parameter instructions, transmitting the pressure parameter instructions to a second device, and actuating a sex toy with the pressure parameter instructions.