A method of delivering a therapeutic and/or diagnostic agent to tissue is provided including the steps of inserting a catheter into a bodily cavity, the catheter having a proximal balloon and a distal balloon, inflating the proximal and distal balloons to create a chamber between the proximal and distal balloons, delivering the therapeutic and/or diagnostic agent to the chamber, measuring fluid pressure in the chamber, measuring at least one fluid dynamic characteristic of a subject, and adjusting the delivery of the therapeutic and/or diagnostic agent based at least in part on the measured volumetric pressure in the chamber and the at least one fluid dynamic characteristic of the subject.

An inflatable system for cervical dilation and labor induction includes a uterine balloon, for positioning at a proximal portion of the uterus, adjacent to the cervical internal os, the uterine balloon being shaped to maximize the pressure against the decidua and the internal cervical os and to minimize the pressure on the fetal head. The inflatable system may have a vaginal balloon, for positioning in the vagina, for applying pressure on the external cervical os. The inflatable system may measure the pressure changes inside the balloon. The inflatable system may have electrodes for measuring the electrical activity of the fetal heart, the maternal heart and the uterine pressure activity and or uterine contractility and or labor progress. The inflatable system may measure cervical dilation, fetal well-being, and the woman's conditions.

Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure sensing elements which may allow for control of the pressure within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled or room temperature fluid such as water may then be used to rapidly terminate the treatment session.

Methods and apparatus for measuring pressure in a patient are provided which may include any number of features. One feature is a pressure measurement system comprising a pressure source, a compliant bladder, a catheter in communication with the pressure source, pressure sensors, and a controller configured to determine a pressure within the compliant bladder. The pressure measurement system can inflate the compliant bladder with gas or air to determine a pressure within a patient. In one embodiment, the pressure measurement system measures pressure within a peritoneal cavity.

A medical valve has a housing with an inlet housing and an outlet housing. The interior of the inlet housing and/or the outlet housing has a contact surface. A resilient element sits within the housing and controls fluid flow through the inlet. The resilient element has a proximal portion with a normally closed aperture configured to open when actuated by a medical device. The resilient element also has a distal portion adjacent to the outlet, and a central portion between the proximal portion and the distal portion. The central portion has a wall that defines a fluid chamber in the open mode and in the closed mode. The wall has at least one projection extending radially outward. The projection maintains compressive contact with the contact surface of the housing and applies an inwardly compressive force on the resilient element, increasing the wall stiffness.

Some embodiments of a balloon catheter device for introduction into a body vessel, in particular the coronary sinus, can include a catheter shaft which carries an inflatable balloon on its distal portion and in which a plurality of different lumens are formed. In particular embodiments, a system for treating heart tissue can include a coronary sinus occlusion catheter configured for improved deliverability to the coronary sinus and for thereafter performing intermittent occlusion of the coronary sinus.

A multi-lumen catheter for monitoring uterine contraction pressure having an elongated body configured and dimensioned for insertion into a bladder of a patient, the catheter having a first lumen, a second lumen, and a first balloon at a distal portion, the first lumen communicating with the first balloon. The second lumen communicates with the bladder to remove fluid from the bladder. The first balloon is filled with a gas to form along with the first lumen a gas filled chamber to monitor pressure within the bladder to thereby monitor uterine contraction pressure of the patient.

A medical tube includes an inner tube shaft which has a proximal end portion and a distal end portion formed at a distal end side of the proximal end portion. The distal end portion has an outer diameter that is smaller than an outer diameter of the proximal end portion, and has on a surface thereof a slit extending in a first direction with respect to a longitudinal direction of the medical tube. The medical tube also includes an outer tube shaft that covers an outer periphery of the distal end portion of the inner tube shaft and has on a surface thereof a slit extending in a second direction crossing the first direction.

A sheath assembly for the insertion of a percutaneous pump includes a tubular sheath body dimensioned for insertion into a blood vessel through a vessel aperture. The tubular sheath body includes a wall having a proximal end portion, a distal end portion, a longitudinal axis, an outer surface, an inner surface defining a first lumen substantially parallel to the longitudinal axis, and a second lumen disposed within the wall between the inner surface and the outer surface and extending from the proximal end portion to the distal end portion. The first lumen is dimensioned to allow passage of a portion of the percutaneous pump, and the second lumen is dimensioned for passage of a guidewire. A stylet is removably positioned to substantially occlude the second lumen. The stylet has a proximal end releasably secured to the sheath assembly.

A pressure-measuring system, including a tube system having at least first and second pressure measuring devices, each including a pressure transducer membrane and a measuring chamber. A first flow regulation device with a perfusion tube section is positioned between the first pressure measuring device and a supply of fluid, and has a first tube clamp that acts on a tube section by squeezing. The system further includes at least one non-perfusion regulation device.