A system for providing neurostimulation includes an external device (“external exciter”) and an implanted device. The external exciter includes an energy source which inductively powers the implanted device. Examples of such external exciters include devices having at least one of: ultrasonic transducers, Radio Frequency (RF) transmitters, and solar cells. The implanted device includes circuitry that limits its maximum energy output to a predetermined saturation threshold such that excess stimulation from the external exciter does not raise the output of the implanted device beyond the saturation threshold. The output signal of the external exciter is then pulse-width modulated in order to produce a desired amount of output stimulation from the implanted device to stimulate the bioelectrically excitable tissue at a desired level.

Ferritin or iron-based image enhancement agents identify target tissue for treatment or ablation and are heated by microwave absorption. Microwave heat substrates enhance microwave hyperthermal ablation treatment, and may be percutaneously delivered and imaged by x-ray CT during placement of the microwave treatment antenna, allowing more precise positioning and more complete ablation of a tumor site. One method of treating a target tissue uses image-guided delivery of a heat substrate with a reverse-phase change polymer, and may apply energy to fix a mass of the material in the tissue. The fixed polymer may increase hyperthermia, form a thermal boundary, or blockade a vessel or passage so as to reduce or prevent undesired conductive cooling by contiguous tissue, or may deliver a localized treatment drug at the site, upon heating or as it degrades over time.

A microwave heat spread apparatus and an operating method thereof are provided. The microwave heat spread apparatus includes: a plurality of antennas respectively disposed at a plurality of positions of the human body and radiating microwaves into the human body; a plurality of channel transceivers respectively connected to the plurality of antennas and configured to transmit and receive the microwaves through a corresponding antenna; a transmission signal distributor configured to distribute a signal to each of the plurality of channel transceivers; a controller configured to control transmission and reception of signals through the channel transceivers; and a detector configured to detect a difference between a signal received through a channel transceiver after passing through the human body and a signal before passing through the human body.

A microwave source used in the radiotherapy device can be provided. The microwave source may include an anode block and one or more cathodes. The cathode of the microwave source may include a cathode support element having a plurality of slots. The plurality of slots can be axially around a circumference of the cathode support element. The microwave source may include a cathode heater including at least one filament. A first part of the at least one filament may be wound around the cathode support element along a first direction and received by a first portion of the plurality of slots, and a second part of the at least one filament may be wound around the cathode support element along a second direction and received by a second portion of the plurality of slots.

A microwave source used in the radiotherapy device can be provided. The microwave source may include an anode block and one or more cathodes. The cathode of the microwave source may include a cathode support element having a plurality of slots. The plurality of slots can be axially around a circumference of the cathode support element. The microwave source may include a cathode heater including at least one filament. A first part of the at least one filament may be wound around the cathode support element along a first direction and received by a first portion of the plurality of slots, and a second part of the at least one filament may be wound around the cathode support element along a second direction and received by a second portion of the plurality of slots.

A microwave device for a disinfection treatment of a human being is disclosed. The microwave device includes a radiation pad including an array of antennas and a microwave generator configured to excite the array of antennas to cause each antenna in the array of antennas to transmit a continuous-wave microwave signal. Each antenna is arranged in the radiation pad so that as the radiation pad is positioned adjacent a treatment area of the human being the continuous-wave microwave signals from the array of antennas combine in the near field in the treatment area to inactivate microbial pathogens comprising bacteria or fungus.

Systems and methods are disclosed for treating back pain associated with a vertebral body of a patient. The system may include an external energy source configured to be positioned at a location external to the body of the patient, a linear configured to drive translation of the external source in one or more axes, a computer coupled to the external source and linear drive and programming executable on said computer for determining a target treatment site within or near the vertebral body based on acquired imaging data, positioning a focal point of the external energy source to substantially coincide with the target treatment site, and delivering a treatment dose of therapeutic energy at said target treatment site, wherein the treatment dose is configured to modulate a nerve within or near the vertebral body.

A neurostimulator implant includes an insulating member and an elongate circuitry unit. The circuitry unit includes (a) a first electrode, disposed on an outer surface of a first end portion of the circuitry unit; (b) a second electrode, disposed on an outer surface of a second end portion of the circuitry unit; and (c) circuitry, disposed inside the circuitry unit, and configured to be wirelessly powered to drive an electrical current between the first and second electrodes. The circuitry unit is disposed alongside a medial part of the insulating member, bulging away from the insulating member to define a generally arced portion of the implant. Lateral parts of the insulating member extend laterally outward from the medial part to define lateral zones laterally beyond the circuitry unit. The second side of the insulating member defines a generally flat side of the implant. Other embodiments are also described.

Devices and methods for treating tissue with microwave energy used in applications such as destroying a soft tissue by microwave ablation and/or creating point, line, area or volumetric lesions. Various embodiments of flexible, low-profile devices are also disclosed where such device can be inserted non-invasively or minimally invasively near or into the target tissue such as cardiac tissue. The devices disclosed herein comprise antennas wherein the field profile generated by an antenna is tailored and optimized for a particular clinical application. The antennas use unique properties of microwaves such as interaction of a microwave field with one or more conductive or non-conductive shaping elements to shape or redistribute the microwave field.

A method for treating the lower extremity varicose vein combined ultrasonic wave and microwave is provided. The method includes steps of firstly finding the diseased vein by the ultrasonic imaging equipment; and then directly effecting the microwave treatment catheter/needle on the diseased vein; by the concentric thermal coagulation release effect of the microwave to the tissue, instantly generating high temperature with the certain penetration range in a small range for tissue coagulation; and then gradually making the vascular fibrosis; finally making the completely atresia, thus achieving the therapeutic aim. The present invention uses the ultrasonic imaging microwave treatment technique to treat the lower extremity varicose vein disease. It accurately, firmly and thoroughly closes the varicose blood vessel, has the exact effect, small trauma and less pain to patients, less bleeding in surgery, quick recovery, simple operative procedure and no significant complication, is difficult to form the deep venous thrombosis.