Abstract:
A laser treatment head guides a laser beam to a target area within a body cavity and includes a laser output element having a deflection element. The laser output element with deflection element is rotatable relative to a guide element about an axis. First and second thread elements mutually engage to cause the deflection element to perform a combined axial and rotational movement relative to the guide element. A control unit and the laser treatment head are configured such that the target area is irradiated by individual pulses (p) in a helical pattern of irradiation spots over a section of the circumference of the body cavity. The control unit is further configured such that reference locations (X) on the target area are irradiated by an individual pulse number (N) of subsequent pulses (p), thereby heating the mucosa tissue within the target area to a predetermined temperature.
Abstract:
The present invention relates to a seating apparatus for the diagnosis and treatment, and more particularly, to a seating apparatus for diagnosis and treatment of diagnosing and curing urinary incontinence, erectile dysfunction and defecation disorders which enables to diagnose symptoms of urinary incontinence, erectile dysfunction and defecation disorders by measuring contraction pressure and contraction duration of pelvic floor muscles, muscles of perineum and anal sphincters of a user, who puts on cloth while seated, simultaneously with curing symptoms of urinary incontinence, erectile dysfunction and defecation disorders throughout biofeedback exercise and training.
Abstract:
A prostate treatment system having a light delivery device positionable in a transurethral device for treatment of benign prostatic hyperplasia (BPH). The light delivery device includes light generator, such as light emitting diodes (LED), laser diodes (LDs) or a diffusion quartz fiber tip connected to a light generator or a light emitting polymer which produces light at a selected wavelength or waveband or alternative sources of suitable light energy. The treatment device may further include a temperature monitoring system for monitoring the temperature at the treatment site. A light-activated drug is administered to the treatment site prior to light activation. The light-activated drug therapy induces cell death of the target tissue. The device provides a minimally invasive transurethral method for treatment of BPH or prostate cancer.
Abstract:
The present invention relates to a photodynamic method of treating prostatic disorders such as BPH. The method comprises: (i) delivering photosensitizer directly into prostatic tissue of a patient suffering from or suspected of suffering from a prostatic disorder; and (ii) irradiating the prostatic tissue with a light at a wavelength appropriate to activate the photosensitizer.
Abstract:
The invention provides a method and system for treating disorders of the genito-urinary tract and other disorders in other parts of the body. A particular treatment can include one or more of, or some combination of ablation, nerve modulation, three-dimensional tissue shaping, drug delivery, mapping, stimulating, shrinking (by creation of a pattern of thermal lesions) and reducing strain on structures by altering the geometry thereof and providing bulk to particularly defined regions. The particular body structures or tissues can include one or more of, or some combination of regions, including the bladder, esophagus, vagina, penis, larynx, pharynx, aortic arch, abdominal aorta, thoracic aorta, large intestine, small intestine, sinus, auditory canal, uterus, vas deferens, trachea and all associated sphincters. In one aspect of the invention, a catheter is deployed in the body. It may enter the body via a natural orifice, a stoma, or a surgically created opening that is made for the purpose of inserting the catheter. Insertion may be facilitated with the use of a guide wire or a generic support structure or visualization apparatus. In second aspect of the invention, the treatment can include application of energy and substances to effect changes in the target tissue. Types of energy that can be applied include radiofrequency, laser, microwave, infrared waves, ultrasound or some combination thereof. Types of substances that can be applied include pharmaceutical agents such as analgesics, antibiotics and anti-inflammatory drugs, bulking agents such as biologically nonreactive particles, cooling fluids or dessicants such as liquid nitrogen for use in cryo-based treatments.
Abstract:
An endoscope, in particular for applications in urology, has a hollow shaft (10), an optical viewing system (12) which can be inserted in the hollow shaft (10) and has a fiber-optic illumination system, an optical fiber (16) which can be introduced with the optical system (12) into the hollow shaft (10) and connected at its proximal end to an external laser source and is bent at its distal end away from the shaft axis. In order to allow irradiation of tissue lying closely packed around the hollow shaft, an indeformable holding tube (14) which is parallel to the optical system (12) and passes through the hollow shaft (10) is provided; this tube accommodates the optical fiber (16) and its distal end is bent at a fixed angle in relation to the shaft axis and accommodated entirely within the shaft cross-section. A spacer (36) with a radiation window (32) ensures that the tissue to be irradiated cannot lie next to the point (18) at which light emerges from the optical fiber (16).
Abstract:
A plurality of embodiments for a flexible probe used to provide photodynamic therapy (PDT) and to effect other medical procedures at an internal treatment site inside a patient's body. Each of the embodiments of the flexible probe (100, 108, 130, 158, 182, 190, 220, 280, 370, 390, 440, 460, 520) includes a flexible substrate (102, 184, 196, 222, 250, 282, 412, 462, 482, 502, 522) on which are disposed conductive traces (414, 466, 468, 488, 490, 504, 506, 524, 526) electrically connected to leads through which electrical current and signals are conveyed. A plurality of light sources (104, 192, 256, 286, 418, 436, 470, 492, 508, 542) or other micro-electronic circuits are connected to the conductive traces and mounted on the flexible substrate. Each of the embodiments of the flexible probes is enclosed within a transparent, biocompatible polymer envelope (106, 110, 464, 522). Due to the characteristic elastic properties of the flexible substrate, the flexible probe can readily be bent, folded, or rolled while being disposed at the internal treatment site. Thus, for example, a curved surgical needle (650) can be used to implant a flexible probe at the treatment site by drawing the flexible probe through tissue along a curved path to a desired position; one or more disk-shaped buttons (660, 670) that are attached to the ends of the flexible probe can be used to secure the flexible probe so that it does not move from the desired position.
Abstract:
A method for the treatment of the prostate gland which heats the tissues which would otherwise be surgically removed with a trans-urethral resection of the prostate. This method is accomplished by combining a radiating energy device integrated with a urinary drainage Foley type catheter, which is modified to provide cooling along the urethra surfaces. The radiating device also serves as a means to measure the tissue radiated thermal energy for the control or monitoring of temperature of the prostate tissues being heated. A urethral inserted applicator for prostate hyperthermia includes a multi-tube, balloon type catheter. The catheter includes a fluid dry tube for an energy radiator antenna applicator which also serves as a radiometric temperature sensor for measuring the temperature of the prostate tissue, and an open fluid receiving tube. An electromagnetic energy generator supplies electromagnetic energy to the applicator. A comparator is connected to the temperature output of the radiometer, and a temperature reference potentiometer for comparing the actual tissue temperature level with a desired temperature level and outputting control signals to the electromagnetic generator for controlling the output to the applicator. The microwave operated applicator is preferably an elongated coil having the tip end connected to the center conductor of a coaxial cable and the opposite end connected to the outer conductor of the coaxial cable. A sheet or sheath of insulation material covers the microwave coil antenna for insulating the coil from the tissue and the thickness of the sheet may be varied to provide uniform tissue heating along the length of the coil. The ultrasound operated applicator is preferably one or more ultrasound crystal cylinders to radiate energy into the tissue and convert tissue thermal ultrasonic energy into electrical energy for measurement by a radiometer, The balloon of the catheter engages the body's bladder to position the applicator properly during the treatment.
Abstract:
The disclosed technology relates to a system for delivering UV-A/B light with a catheter to treat infectious or inflammatory disorders in a patient. While UV light in the UV-C range has traditionally been used to treat skin disorders and for focused ablation of plaques in the arteries and other targeted internal uses, it has not been developed for broader infection, inflammation or neoplasia treatment inside the human body. Here, the inventor(s) developed a system for emission of therapeutic doses of UV light via a catheter, capsule, endoscope, tube or port that can be used to manage internal infections and inflammatory conditions inside a patient.
Abstract:
A light-emitting, antimicrobial tuber, instrument or catheter includes a thin, flexible tube having an optically transparent wall; and a light transmitter configured and arranged to emit light through the tube, which may be ultraviolet C (UVC) irradiation, photodynamic therapy (PDT), violet-blue light therapy, and other light-based therapies. In one embodiment, violet-blue light from 400-500 nm in wavelength, such as 405 nm, for instance, is used. The device is used on a patient and a therapeutic amount of light is administered to the patient, thereby reducing the risk of infections being transmitted from the instrument, tube or catheter to the patient, generally. The device may be configured for use in the urinary tract or as intravascular, and may be indwelling or temporary. Light may be administered for the duration of use or another time period effective to halt, inhibit, or reduce microbial or fungal growth.