Abstract: A method is provided including placing a nerve stimulator implant at an implant location in a patient's body in a vicinity of a target nerve. The nerve stimulator implant is activated to apply electrical stimulation to the target nerve. The following indications are received from the patient: (a) a remote-paresthesia indication of a presence or an absence of remote-site paresthesia caused by the electrical stimulation at a predetermined remote-paresthesia site of the body that is remote from the implant location, and (b) an adverse-effect indication of a presence or an absence of an adverse sensation caused by the electrical stimulation at an adverse-sensation site of the body that is not innervated by the portion of the target nerve. Depending on the indications, the nerve stimulator implant is adjusted, the implant location is adjusted, or the implantation of the nerve stimulator implant is completed without adjustment. Other embodiments are also described.

Abstract: Apparatus includes an implant and an introducer. The implant includes an injectable housing, an electrode disposed on an outer surface of the housing, and circuitry. The circuitry is configured to alternate between a first mode in which the circuitry drives the electrode to apply a first electrical current having a frequency of 1-100 Hz, and a second mode in which the implant applies a second electrical current having a frequency of 1-10 kHz. The introducer includes a tube that defines a lumen and is percutaneously-advanceable into tissue of the subject, the lumen being dimensioned to at least temporarily house the implant. The introducer is configured to deploy the implant from a distal end of the lumen by moving the implant and the distal end of the lumen relative to each other. Other embodiments are also described.

Abstract: Apparatus includes an implant and an introducer. The implant includes an injectable housing, an electrode disposed on an outer surface of the housing, and circuitry. The circuitry is configured to alternate between a first mode in which the circuitry drives the electrode to apply a first electrical current having a frequency of 1-100 Hz, and a second mode in which the implant applies a second electrical current having a frequency of 1-10 kHz. The introducer includes a tube that defines a lumen and is percutaneously-advanceable into tissue of the subject, the lumen being dimensioned to at least temporarily house the implant. The introducer is configured to deploy the implant from a distal end of the lumen by moving the implant and the distal end of the lumen relative to each other. Other embodiments are also described.

Abstract: An electrostimulator implant is percutaneously advanceable into tissue of a limb of a subject. The implant comprises (i) an intracorporeal sensor, configured to detect a factor indicative of local blood supply in the tissue of the limb; (ii) an electrode disposed at an outer surface of the implant; (iii) an antenna, configured to wirelessly receive power; and (iv) circuitry, powered by the received power, and configured to drive the electrode to apply a bloodflow-increasing current to the tissue at least in part responsively to the detected factor. Other embodiments are also described.

Abstract: An electrostimulator implant is percutaneously advanceable into tissue of a limb of a subject. The implant comprises (i) an intracorporeal sensor, configured to detect a factor indicative of local blood supply in the tissue of the limb; (ii) an electrode disposed at an outer surface of the implant; (iii) an antenna, configured to wirelessly receive power; and (iv) circuitry, powered by the received power, and configured to drive the electrode to apply a bloodflow-increasing current to the tissue at least in part responsively to the detected factor. Other embodiments are also described.