This application relates to a hand-held cooling device for supplying a cryogen to a target region for cryotherapy. The device can include a cryogen transfer unit configured to receive a first cryogen from an external cryogen reservoir, the first cryogen including i) a first amount of a liquid phase cryogen and ii) at least one of a first solid phase cryogen and a first gas phase cryogen. The device can also include a nozzle configured to spray a first modified cryogen to the target region. The device can further include a cryogen liquefier disposed between the cryogen container and the nozzle and configured to cool the first cryogen received from the cryogen transfer unit and output the first modified cryogen to the nozzle, the first modified cryogen including at least a second amount of the liquid phase cryogen more than the first amount of the liquid phase cryogen.

The present invention provides a nasopharyngeal airway management device for brain-nasal cavity cooling according to the present invention including a cooling gas induction hose that is a tubular body with a hollow inside along a length, and induces a cooling gas introduced through one side to the other side; an adapter that is connected to the other side of the cooling gas induction hose, is mounted around the patient's upper lip, distributes the cooling gas induced through the cooling gas induction hose to a pair of discharge ripples, and discharges the cooling gas; and a nasal cavity cooling tube that is a tubular body with a hollow inside along a length, one side is coupled to a discharge nipple of the adapter and the other side of which is inserted into the patient's nasal cavity, and forms a plurality of discharge holes for discharging the cooling gas to any one point of the length, so that the nasal cavity cooling tube that is connected to the adapter fixed to the patient's upper lip, and dividing and discharging the cooling gas introduced through the cooling gas induction hose is inserted into the nasopharynx through the patient's nostril, and the cooling gas (low-temperature oxygen) discharged through the discharge hole of the the nasal cavity cooling tube is discharged into the nasal cavity close to the brain, and thereby quick and easy stable local cooling of the brain is induced while maintaining the nasopharyngeal airway.

The thermal treatment device is primarily to be wrapped about one's neck. The thermal treatment device is an elongated container, like a sleeve, having two sides that may be air permeable. The container has one or more aligned pockets capable of holding gel packs. A source of power is placed in one pocket of the container and has on-off switch. Also included is a microfan device being placed in a pocket and receiving power from the source of power. The microfan device has air outlet and air inlet openings thereabout. The microfan blades are positioned between a top row of air inlet holes and a bottom row of air outlet holes. The microfan blows air into the gel pack pockets past the cooled gel packs and then exits through the one or more air permeable sides to cool the user. The gel packs may be removable.

At least some aspects of the present disclosure feature a convective system including an inflatable convective device and a manifold. The inflatable convective device has a pneumatic structure and two openings into the pneumatic structure. The hose manifold includes a hose connector configured to connect to a hose, two outlet connectors configured to connect to the two openings respectively, where the hose connector and the two output connectors are in fluid connection.

A system and method for automatically producing and monitoring a cryotherapy session within a chamber includes a plumbing system coupled to the chamber for cooling the chamber. A central controller may be coupled to the plumbing system. The central controller may be operable for: initiating the cryotherapy session within the chamber with a cryogenic gas flowing through the plumbing system for cooling the chamber to a first temperature; determining if the first temperature has been reached within the chamber; determining if a check-in command has been received for the cryotherapy session; and stopping the cryotherapy session after a predetermined period of time. The central controller may initiate a pre-cooling session for cooling the chamber to a second temperature which is different than the first temperature; and determine if the second temperature has been reached in the chamber. The pre-cooling session generally occurs prior to the cryotherapy session for removing ambient heat.

Systems and methods provide air or gas-based temperature-controlled medical devices. The systems and methods may be applied to provide therapy to a patient suffering orthopedic or other injuries. Air or other gas is temperature-controlled and adjusted to meet a patient's physical needs and delivered the patient therapy site through a temperature regulated system including a therapeutic orthopedic wrap. Feedback mechanisms allow the caregiver or the patient to adjust the temperature of the gas. Other fluids may also be used. The systems and methods permit use of electrotherapy for enhanced therapy and injury recovery.

Refers to equipment (E), the objective of which is to take extremely cold air to a cap (1) comprised by a cylindrical duct (2), located in the upper part of the cylindrical structure (3) of the cap (1) which is coated by a thermal foam (ESP) and any given material (M), wherein the cylindrical duct (2) overlaps a sprinkler (ASP), which is located in the inner part (I) of the cylindrical structure (3) of the cap (1), further, the cap (1) comprises fins (4) which form an angle of 90 in relation to the inner walls (I) of the cylindrical structure (3) of the cap (1), which finally also has reinforcement ribs (5) and a circular support (6) endowed with a central hollow (7) circular and/or oval coated by a thermal foam (ESP) throughout its perimeter.

A combination therapy pad that includes a first layer and a second layer operatively coupled to the first layer. A fiber-optic array is disposed between the first layer and the second layer. A third layer is operatively coupled to the first layer. The third layer includes a vacuum tube in fluid communication with a vacuum source and a therapeutic fluid tube in fluid communication with a therapeutic fluid source. The third layer provides at least one of vacuum therapy and therapeutic fluid treatment to a wound area.

The air flow system includes a hose member having an exterior flow tube and an interior flow tube, a distal connector, and a proximal connector. The air flow in the interior flow tube is separate from the exterior flow tube. Air flows from the exterior flow tube, through a flow chamber, around a treatment site of inflammation and back to the interior flow tube. The system for air circulation therapy also includes a body attachment device, an air pump supply, an air recovery unit, a temperature sensor, an air flow sensor, and a controller. The method includes inserting a body part with a treatment site within the flow chamberand sealing the flow chamber to the air flow system. Temperature regulated air flow is supplied to the treatment site in the flow chamber and collected from the flow chamber.

An electronically controllable pillow is thermally regulated. At least one temperature sensor is configured to communicate temperature measurements. Temperature measurements comprise the internal temperature of a pillow. Temperature measurements are communicated to a processing unit. At least one presence sensor is configured to communicate presence measurements. Presence measurements are configured to indicate the presence of a user employing a pillow. Presence measurements are communicated to a processing unit. At least one transceiver is connected to a processing unit. A transceiver is configured to communicate with at least one remote device. At least one thermal element is activated, based at least in part on, temperature measurements and presence measurements over at least one period of time.