A pressure-sensing device includes a device frame, a flexible membrane, a pressure sensor, and device electronics. The device frame includes a base surface that rests on a supporting structure and a frame attachment region located opposite to the base surface such that the frame attachment region is raised from the supporting structure when the base surface is resting on the supporting structure. The device frame also includes a seating surface. The flexible membrane is attached to the frame attachment region such that the device frame and the flexible membrane enclose a pressure chamber. The seating surface extends outward around the flexible membrane and the flexible membrane protrudes above the seating surface. The pressure sensor is configured to generate a pressure signal. The device electronics are configured to determine the pressure in the pressure chamber based on the pressure signal.

The present invention relates to an apparatus for strengthening pelvic floor muscles which can be used even when a user wears clothes and thus can be used comfortably without psychological burden; can be cleanly used without the remains of foreign matter around the urethra and the anus or on the exterior of the apparatus after use; can perform treatment in a state in which an electrode portion is pressed in close contact with the bladder and the pelvic floor muscles through a height adjustment means; and can perform both an active exercise through low-frequency pulses and a passive exercise through a muscular strength sensing means.

Featured are intravaginal devices and electrical stimulation devices, systems, thereof, and methods of using the devices and systems thereof to observe pelvic floor movements in order to diagnose, treat, or prevent urinary and fecal incontinence disorders (e.g., urge incontinence) and their accompanying symptoms or to diagnose and/or improve the efficacy of neuromodulation therapy.

A Kegel exercise measurement and feedback device measures the amount of force that is exerted on a sensor portion and provides feedback in the form of vibration, a phrase or a light that is emitted from a feedback module. A sensor portion comprises a resilient body having a bladder in an inner cavity that can be compressed by Kegel exercises. Air within the bladder is forced into a bellows of the measurement portion which expands the bellows and a contactor plate attached thereto. As the contactor plate moves, due to the expansion of the bellows, it makes contact with level contactors to activate a corresponding feedback phrase, emitted light or vibration. The phrases emitted may be phrases recorded by a user and stored in memory or may be pre-loaded into memory. The sensor portion may be detachable from the measurement portion of connection conduit.

The self-contained endocavitary probe device for managing stress incontinence is capable of being inserted into the vaginal or rectal cavity of a person. The device includes at least one self-contained electrical power supply so as to supply power to at least one device for measuring the variation in a parameter resulting from physical stress and to at least one electrical muscle stimulation device in contact with at least one muscle capable of maintaining urinary continence. The electrical stimulation device is activated in the event of variation in the parameter.

A method for detecting disease using a manometry includes obtaining pressure values from each of the plurality of pressure sensors during a pre-set time, obtaining a three-dimensional pressure distribution showing the changes in the pressure values according to location and time by using the time, the pressure values, and locations in which the pressure sensors are disposed within the arbitrary location section, and calculating the volume integral value of the interest location which is predetermined in accordance with the disease, in the three-dimensional pressure distribution.

Featured are intravaginal devices and methods of using the devices to observe the state of an individual's pelvic floor muscles in order to diagnose, treat, or prevent pelvic floor disorders (e.g., pelvic organ prolapse and incontinence) and their accompanying symptoms and methods of using the devices to treat or prevent vaginal disorders (e.g., skin laxity) in a subject using an energy transmitter (e.g., a radiofrequency transmitter).

A device for measuring contractions and/or relaxation of one or more muscles of a body cavity, the device having a hollow body which is for positioning in the body cavity and which is covered by a coating made of or having a biocompatible material, the body being formed of two half-shells which are each physically connected, permanently and continuously during the use of the device, with the aid of non-compressible or deformable connecting means, to at least one pressure sensor, or part of the pressure sensor, arranged in the body. Also, a method for measuring the contraction and/or relaxation of the muscles of a body cavity, a method for monitoring the contractions and/or relaxation of the muscles, and a method for exercising these muscles.

A non-transitory tangible computer-readable medium or media include one or more sequences of instructions which, when executed by one or more processors, causes steps to be performed, where the steps include receiving data obtained from baseline clinical evaluation and a urodynamic test for a patient, the diagnostic engine having been trained to associate a data obtained from a urodynamic test with one or more lower urinary tract dysfunction; extracting one or more features from the received data; identifying one or more urodynamic parameters of the patient's lower urinary tract dysfunction, based on the one or more extracted features; and generating an output that includes information of one or more lower urinary tract dysfunction associated with the one or more identified urodynamic parameters.

A balloon assembly for an anorectal manometry catheter may include a three-part tube and a balloon mountable on the tube. The three-part tube may include a flexible proximal connection tube (PCT), a flexible distal connection tube (DCT), and a semi-flexible transfer tube that is interposed between and connected to each of said PCT and said DCT. The balloon may have a first opening connected to a first end of the transfer tube and a second opening connected to a second end of the transfer tube which is opposite the first end of the transfer tube. The three-part tube may be configured to be slidable along and over a catheter in a first direction, with the DCT slid first. The three-part tube may also be configured to be slidable over the catheter in the opposite direction such that the PCT is folded onto itself and completely contained in the transfer tube.