A system and method for providing Thermal contrast therapy are presented. The system may comprise a fluid membrane barrier, a human interface device (HID), fluid tubing, a pump, and a reservoir. The system may be operable to apply any combination of heat, cold, and pressurized compression, light energy, acoustic energy, and vibratory energy to a therapy recipient for treating anal-prostate-perineal and vaginal areas, as well as podological and other extremities. The system may be operable to impart a desired therapy temperature to the human interface device and to expand a membrane containing a therapy fluid. The expanded membrane may conform to the contours of a therapy site. Operation of the human interface device may be controlled using a remote-control device. The therapy recipient may be able to control the temperature of the fluid or gel, as well as reception of light energy, acoustic energy and vibratory pulsing energy to assist in treatment of one or more conditions.

Disclosed are devices and methods for body temperature management using a heat transfer catheter carrying a heat transfer fluid to heat or cool a desired, focused portion of a patient's body. In accordance with certain aspects of the invention, the heat transfer catheter may include hollow nodes that have greater rigidity than the remainder of the catheter to aid in placement of the heat transfer catheter within and navigation of the desired portion of the patient's body. Methods of using such heat transfer catheter to effect temperature management of the patient's body are also disclosed.

An endorectal cooling device (ECD) includes an elongated body, a cooling fluid circuit, and a gas bubble removal device. The elongated body includes an insertable portion for insertion into a patient's rectum and an external portion that remains external to the rectum. The cooling fluid circuit is defined in the elongated body from the external portion to the insertable portion and circulates cooling fluid to regulate a temperature of a cooling surface on the insertable portion. The gas bubble removal device can include a coil, a tube, a mesh, and/or a hole that is disposed on or defined in the insertable portion of the elongated body, such as the cooling surface. A low-pressure source, such as a vacuum pump or a Venturi structure, can be fluidly coupled to the gas bubble removal device to remove fluid and bubbles by a suction force after the ECD is inserted into the rectum.

A device and method to treat an overgrowth of yeast in a body cavity and inflammatory and/or hemorrhagic conditions of a body cavity. The device comprising a shell, removal means, and a freezable filler contained in a chamber within the shell. When the filler is frozen and the device inserted into the body cavity, the shell cools the body cavity to a temperature that inhibits the replication of yeast and provides relief to symptoms. An external cooling component extending from the shell provides cooling at the body cavity opening, An expandable bladder in the shell provides tamponade treatment for body cavity hemorrhaging.

Devices, system and methods for heating pelvic floor tissues are provided. The devices of the present invention can be used to apply heat to pelvic floor tissues such as rectal, vaginal, urethral and/or bladder tissues in order to treat disorders associated with such tissues.

A perineal heating pad includes a central portion and two opposing end portions. The central portion includes a heating element disposed on or within the heating pad and the opposing ends may include one or more tabs extending outward from the central portion. A non-stick adhesive is used to secure the heating pad to the perineal body tissue of the patient and a controller supplies heat to the heating element and maintains the perineal tissue of a patient at a desired temperature.

A device and method to treat an overgrowth of yeast in a body cavity and inflammatory and/or hemorrhagic conditions of a body cavity. The device comprising a shell, removal means, and a freezable filler contained in a chamber within the shell. When the filler is frozen and the device inserted into the body cavity, the shell cools the body cavity to a temperature that inhibits the replication of yeast and provides relief to symptoms. An external cooling component extending from the shell provides cooling at the body cavity opening. An expandable bladder in the shell provides tamponade treatment for body cavity hemorrhaging.

A hot air producing system produces and stores hot air, and applies the stored hot air to a human body. The system includes a heating apparatus to heat the air, a temperature setting gauge to allow a user to set a desired temperature, a pressure gauge to measure a pressure of the air in the container, a pump to pump the hot air, a fill connection, an expandable container for receiving and storing the hot air, with a valve to connect to the fill connection such that the expandable container can receive the hot air, an adjustable flow release mechanism to allow a user to adjust an amount of flow of hot air out of the expandable container, and a flexible hose connected to the adjustable flow release mechanism, with a nozzle to direct the hot air to a portion of the human body.

A system and method for providing Anal Perineal Prostate Vaginal Pelvic Floor contrast therapy are presented. The system may comprise a human interface device, fluid tubing, a pump, and a reservoir. The system may be operable to apply any combination of heat, cold, and pressurized compression to a therapy recipient and demonstrates particular utility for treating anal-prostate-perineal and vaginal areas. The system may be operable to impart a desired therapy temperature to the human interface device and to expand a membrane containing a therapy fluid. The expanded membrane may conform to the contours of a therapy site. Operation of the human interface device may be controlled using a remote-control device. The therapy recipient may be able to control the temperature of the fluid circulating through the membrane and may be able to control the pressure of the fluid within the membrane.

An assembly for gluteal cleft moisture reduction including a case having a plurality of walls, the case being opened by an air input port; an air tube having upper and lower ends wherein the tube's upper end forms a dorsal extension communicating with an opening in the flexible skin contact plate mounted on the case, the plate ventrally overlying the air tube; an air conduit housed within the case, the conduit having input and output ends communicating with the case's air input port and with the air tube; an electric motor and air impeller combination housed within the case, the combination being adapted for moving air through the air conduit; an electric battery within the case; and a matrix of electric conductors operatively interconnecting the electric motor and the electric battery.