Abstract: A method is disclosed for treating a living body tissue by cauterizing a sympathetic nerve around a renal artery to block a neurotransmission function of the sympathetic nerve. The method includes inserting a balloon catheter including a balloon on a distal end side of a shaft into a body cavity, and delivering the balloon to the renal artery; inflating the balloon that has been delivered to the renal artery; puncturing a blood vessel wall with at least one protrusive member disposed on an outer surface of the balloon when the balloon is inflated; and after puncturing the blood vessel wall with the protrusive member, cauterizing the sympathetic nerve within a region at a periphery of an electrode disposed on a projecting tip end portion of the protrusive member by supplying a current to the electrode.

Abstract: A stent for placement in living body is substantially in a tubular form and includes a plurality of wave-shaped struts extending in the axial direction from one end to the other of the stent. The axially-extending wave-shaped struts are arranged in a circumferential direction, and connection struts interconnect the respective circumferentially adjacent wave-shaped struts. The circumferentially adjacent wave-shaped struts include a plurality of closer sections and farther sections. The connection struts interconnect between the closer sections of adjacent wave-shaped struts, and each has at the center thereof a bent portion extending in the axial direction of the stent.

Abstract: A method is disclosed for treating a living body tissue by cauterizing a sympathetic nerve around a renal artery to block a neurotransmission function of the sympathetic nerve. The method includes inserting a balloon catheter including a balloon on a distal end side of a shaft into a body cavity, and delivering the balloon to the renal artery; inflating the balloon that has been delivered to the renal artery; puncturing a blood vessel wall with at least one protrusive member disposed on an outer surface of the balloon when the balloon is inflated; and after puncturing the blood vessel wall with the protrusive member, cauterizing the sympathetic nerve within a region at a periphery of an electrode disposed on a projecting tip end portion of the protrusive member by supplying a current to the electrode.

Abstract: A blood vessel insertion-type treatment device and method of cauterizing biological tissues are disclosed. The blood vessel insertion-type treatment device having a first torque transmission body and a first ultrasonic generator. The first torque transmission body has a longitudinal shape and having a proximal end and a distal end. The first torque transmission body transmits a torque which is supplied to the proximal end and which pivotally rotates the first torque transmission body in a longitudinal direction of the longitudinal shape. The first ultrasonic generator is disposed in the first torque transmission body. The first ultrasonic generator radiates ultrasonic waves for cauterizing biological tissues, which are apart from the first ultrasonic generator by a predetermined distance.

Abstract: A blood vessel insertion-type treatment device has a first ultrasonic transmitter and an insertion body. The first ultrasonic generator has a first ultrasonic transducer and a first actuator. The first ultrasonic transducer radiates cauterizing ultrasonic waves converging on a converging position. The first actuator 108 adjusts a direction of the converging position with respect to the first ultrasonic transducer. The insertion body has a longitudinal shape whose both ends have a proximal end and an insertion end. The first ultrasonic generator 106 is disposed near the insertion end in the insertion body.

Abstract: An ablation device includes a waveguide that guides a pulse laser output from a laser output unit, a laser emitting unit that focuses the pulse laser guided by the waveguide using a lens, emits the pulse laser to a living body tissue, causes multiphoton absorption in a focal position of the pulse laser, and performs ablation on the living body tissue; and a balloon that sets a focus of the pulse laser as the laser emitting unit is positioned at a desired position inside a living body lumen.

Abstract: A stent delivery system includes a self-expanding stent, an inner tube body which has a guide wire lumen, and a sheath which has the stent contained within the tip section thereof. The stent can be discharged by moving the sheath to the base end side relative to the inner tube body. The inner tube body is provided at a position within the base end section of the stent and is provided with an elastic member for pressing the stent in the direction to the sheath. The stent is gripped by the elastic member and the sheath and is adapted to be slidable relative to the sheath.

Abstract: A balloon catheter is provided with a balloon on the tip of a main shaft. The balloon catheter is provided with: protruding parts that are furnished on the outer surface of the balloon and protrude outward from the outer surface of the balloon at least when the balloon is expanded; and electrodes that are furnished on the leading edges of the protruding parts in the direction of protrusion and are capable of transmitting energy to living tissue. The leading edge electrodes can thereby be delivered near the desired site of treatment by thrusting the protruding parts into living tissue and, in this configuration, energy is transmitted to said treatment site.

Abstract: A stent includes a plurality of first wave-shaped struts extending in the axial direction of the stent and arranged in the circumferential direction of the stent, a plurality of second wave-shaped struts each located between the first wave-shaped struts, and one or more connecting struts each interconnecting the first wave-shaped strut and the second wave-shaped strut which are adjacent to each other, with the one or more connecting struts extending in the axial direction over a predetermined length. The apexes of the second wave-shaped struts are shifted a predetermined distance in the axial direction of the stent relative to the apexes of the first wave-shaped struts which are located close to the apexes in the circumferential direction of the stent and which are curved in the same direction as the apexes.

Abstract: A stent delivery system includes a self-expanding stent, an inner tube body, and a sheath whose distal portion contains the stent. The stent can be discharged by moving the sheath proximally relative to the inner tube body. The inner tube body includes a distal contact section provided relative to a proximal portion of the stent and does not enter side wall openings of the stent; and a proximal contact section located at a position rear of the proximal end of the stent and close to the distal contact section. The stent has a proximal inwardly protruding section which can make contact with the distal contact section of the inner tube body. The proximal inwardly protruding section is located between the distal contact section and the proximal contact section. The stent does not, except in the proximal portion thereof, have a substantially bent, free end which protrudes towards the proximal side.

Abstract: A stent delivery system includes a stent formed in a substantially hollow cylindrical shape and compressed toward its center axis when inserted in vivo, with the stent being capable of restoring its pre-compression shape through outward expansion when left indwelling in vivo. The stent delivery system also includes an inner tube possessing a guide wire lumen, and a stent accommodating tube having a distal portion accommodating the stent. The stent is disposed as to cover a distal portion of the inner tube, and the stent is adapted to be exposed by moving the stent accommodating tube toward the proximal side relative to the inner tube.

Abstract: A stent delivery system includes a body and an operation unit disposed at the proximal end of the body. The body includes a self-expanding stent, an inner tube body, and a stent-accommodating tube body in which the stent is accommodated. The inner tube body has a stent-holding part enabling the stent to be re-accommodated into the stent-accommodating tube body. The operation unit includes a rack member fixed to a proximal end of the stent-accommodating tube body, an operation rotary roller having a working gear wheel that engages the teeth of the rack member, thereby causing the rack member to move forward and backward; and a connector fixed to a proximal end portion of a proximal-side tube that penetrates the stent-accommodating tube body and protrudes from the proximal end of the stent-accommodating tube body.

Abstract: A stent delivery system includes a self-expanding stent, an inner tube body which has a guide wire lumen, and a sheath which has the stent contained within the tip section thereof. The stent can be discharged by moving the sheath to the base end side relative to the inner tube body. The inner tube body is provided at a position within the base end section of the stent and is provided with an elastic member for pressing the stent in the direction to the sheath. The stent is gripped by the elastic member and the sheath and is adapted to be slidable relative to the sheath.

Abstract: A stent for placement in living body is substantially in a tubular form and includes a plurality of wave-shaped struts extending in the axial direction from one end to the other of the stent. The axially-extending wave-shaped struts are arranged in a circumferential direction, and connection struts interconnect the respective circumferentially adjacent wave-shaped struts. The circumferentially adjacent wave-shaped struts include a plurality of closer sections and farther sections. The connection struts interconnect between the closer sections of adjacent wave-shaped struts, and each has at the center thereof a bent portion extending in the axial direction of the stent.

Abstract: A stent includes a plurality of first wave-shaped struts extending in the axial direction of the stent and arranged in the circumferential direction of the stent, a plurality of second wave-shaped struts each located between the first wave-shaped struts, and one or more connecting struts each interconnecting the first wave-shaped strut and the second wave-shaped strut which are adjacent to each other, with the one or more connecting struts extending in the axial direction over a predetermined length. The apexes of the second wave-shaped struts are shifted a predetermined distance in the axial direction of the stent relative to the apexes of the first wave-shaped struts which are located close to the apexes in the circumferential direction of the stent and which are curved in the same direction as the apexes.

Abstract: A stent delivery system includes a self-expandable stent, a shaft section having a guide wire lumen, and a sheath having distal portion containing the stent. The stent is located at a position which is on the shaft section and near the distal end of the shaft section. The stent delivery system has a stent proximal portion fixing wire and a breaking member. The stent proximal portion fixing wire has one end portion and the other end portion which are fixed to the shaft section, and also has an intermediate portion engaged with a proximal portion of the stent. The breaking member breaks the stent proximal portion fixing wire to release the stent from the engagement.

Abstract: A stent delivery system includes a stent formed in a substantially hollow cylindrical shape and compressed toward its center axis when inserted in vivo, with the stent being capable of restoring its pre-compression shape through outward expansion when left indwelling in vivo. The stent delivery system also includes an inner tube possessing a guide wire lumen, and a stent accommodating tube having a distal portion accommodating the stent. The stent is disposed as to cover a distal portion of the inner tube, and the stent is adapted to be exposed by moving the stent accommodating tube toward the proximal side relative to the inner tube.

Abstract: An implantable tubular device is formed as a substantially tubular body and has a deformable portion formed on a peripheral surface thereof, with the deformable portion forming a predetermined angle with respect to an axial direction of the implantable tubular device. The implantable tubular device includes a plurality of wavy annular members each formed of a wavy element and arranged in an axial direction of the implantable tubular device; and connection portions each connecting the wavy annular members to each other in the axial direction of the implantable tubular device. Each of the wavy annular members has a deformable portion 11 formed on a bent portion thereof not connected to the other wavy annular members in such a way that the deformable portion crosses the wavy annular member.

Abstract: There are provided an implantable medical material composed of an angiotensin II receptor antagonist and a biocompatible material or a biodegradable material, which can be applied to an injury lesion of the blood vessel and the like directly and locally, and can reliably suppress the proliferation of smooth muscle cells and prevent restenosis of the blood vessel and the like, and implantable medical device composed of the medical material and a holder.

Abstract: An implantable tubular device is formed as a substantially tubular body and has a deformable portion formed on a peripheral surface thereof, with the deformable portion forming a predetermined angle with respect to an axial direction of the implantable tubular device. The implantable tubular device includes a plurality of wavy annular members each formed of a wavy element and arranged in an axial direction of the implantable tubular device; and connection portions each connecting the wavy annular members to each other in the axial direction of the implantable tubular device. Each of the wavy annular members has a deformable portion 11 formed on a bent portion thereof not connected to the other wavy annular members in such a way that the deformable portion crosses the wavy annular member.