A tape 400 or wrap is provided which includes first and second elongated elastic layers 345, 346 sized to conform to the shape of a portion of the external skin of the body of a wearer; and a heated area comprising an exothermic material 310 sandwiched between said first and second elastic layers 345, 346, wherein said exothermic material 310 is activated by exposing said exothermic material 310 to oxygen; wherein said tape 400 or wrap has a elasticity of at least about 10-90% and said heated area is capable of substantially expanding and contracting with the tape or wrap. Methods of using the tape 400 or wrap are also provided.

A therapeutic garment for cooling an arm of a user includes a vest that is configured to position over a torso of the user. A sleeve is coupled to and extends from a circumference of an armhole of the vest so that the sleeve is configured to insert the arm of the user. The sleeve comprises an inner layer that is coupled to an outer layer so that the inner layer and the outer layer define an interior space. The interior space extends from a cuff of the sleeve to the armhole. An orifice is positioned in the outer layer proximate to the armhole. The orifice is configured to selectively insert a cooling material into the interior space, positioning the cooling material to cool the arm of the user. A closure is coupled to the outer layer proximate to the orifice and is positioned to selectively and sealably close the orifice.

A method for anesthetizing a human patient undergoing surgery and/or pain block procedure, the method comprising sterilizing the patient's skin including a target region, the target region including a surgical site including the patient's spine; inserting at least one cryo-needle into a first tissue region, the cryo-needle having a distal end configured to cool surrounding patient tissue, the first tissue region comprising soft tissue superficial to the one or more vertebra and on a first lateral side of the patients spine; cooling the distal end of the cryo-needle to cause cooling of surrounding patient tissue thus inhibiting one or more sensory nerves in the surrounding patient tissue; thereafter, performing spinal surgery on the patient's spine at the surgical site; and, thereafter, performing an erector spinae plane block to further inhibit nerves post-operatively in the target region.

A lightweight, portable, cost-effective skin-cooling device is adapted for use with a coolant spray in an existing canister having a rim surrounding a push-activated spray tube. The apparatus comprises a housing with an inlet end that snaps onto the existing canister, an outlet end with a skin-contacting component, and a pushbutton. A tubular structure, disposed within the housing, includes an inlet end configured to engage with the push-activated spray tube of the canister, and an outlet end directed toward the skin-contacting component supported over the outlet end of the housing. Depressing the pushbutton causes the inlet end of the tubular structure to depress the push-activated spray tube, thereby causing the coolant spray to be carried though the tubular and out the outlet end thereof to cool the skin-contacting component.

A method in which a location is determined on the skin that is proximate to a sensory nerve that is associated with a painful condition. At least one needle of a cryogenic device is inserted into the location on the skin such that the needle is proximate to the sensory nerve. The device is activated such that the at least one needle creates a cooling zone about the sensory nerve, thereby eliminating or reducing severity of the painful condition.

The invention provides a cooling pad 110 for alleviation of pain or discomfort, especially in the perineum as a result of childbirth. The pad 110 has at least one chamber 116 containing a fluid (such as saline) for cooling. There is at least one aperture 126 for allowing passage of body fluid. The aperture 126 is located inboard of the chamber 116.

Aperture 126 is formed in a web 124.

Cooling pad 110 may be used alone or as part of an assembly, sandwiched between cover layer 130 and peel-off backing 132, and is intended to be placed in a freezer prior to use.

An economical dual modality system is useful in a system for independent delivery of two distinct energy modalities to a mammalian body and includes a thermal subsystem. The thermal subsystem includes a thermal source affixed to flexible web having an adhesive surface and at least one structure arranged and configured to couple the thermal subsystem to a chassis comprising a durable energy subsystem.

The present invention relates to a pad for treating skin diseases, comprising agar gel and a fiber layer fixed to the inside of the gel, and a manufacturing method therefor. The pad of the present invention inhibits blood vessel exudation symptoms according to vasodilation by maintaining a low temperature of the affected area, reduces an itchy sensation and, at the same time, removes, from the skin, plasma proteins and various plasma-derived substances accumulated in skin tissue, thereby having an effect of alleviating the symptoms of the affected area.

A system and method for portably delivering a therapeutic dose of heat to the skin to relieve pain, reduce accommodation of thermal nerve receptors, promote healing, and deliver transcutaneous medications. The heating device is user programmable or pre-programmed to deliver according to a variety of cycles, patterns and algorithms. The cycles, patterns, and algorithms of the heat are programmable parameters, are under the user's control, and increase the effectiveness and efficiency of the device. The heating algorithms are designed to interact with an individual users thermal nerve receptors and other tissue characteristics and to reduce the tendency of the receptors to accommodate to the external stimuli with back pain, muscular pain, dysmenorrhea, headaches, fibromyalgia, post-herpetic neuralgia, nerve injuries and neuropathies, and sprains and strain. The device can also be used in conjunction with existing medical devices such as Transcutaneous Electrical Nerve Stimulators (TENS) to increase the effectiveness of TENS devices.

A therapeutic splint for the treatment of one or more joint areas of a patient. The splint includes longitudinal housings extending along a longitudinal axis (L) and arranged parallel to this longitudinal axis (L); one or more modular cartridges with therapeutic effect suitable for being arranged in the housings according to the joint area (s) to be treated. The splint further includes at least one transverse and/or oblique housing extending along one or more transverse and/or oblique axes (O), respectively, with respect to the longitudinal axis (L) of the splint. The transverse and/or oblique housing is arranged so as to cover an area extending around a joint to be treated. The modular cartridge or cartridges are arranged in the transverse and/or oblique housings according to the joint area(s) to be treated.