US2022151675A1PendingUtilityA1

Medical devices utilizing shape memory alloys and associated systems and methods

Assignee: BRANDNER THERESAPriority: Apr 14, 2016Filed: Feb 7, 2022Published: May 19, 2022
Est. expiryApr 14, 2036(~9.7 yrs left)· nominal 20-yr term from priority
A61B 18/1482A61L 31/022A61B 2018/00559A61B 2018/1407A61B 18/1492A61F 2210/0014A61B 2018/00494A61B 2018/00488A61B 2018/00095A61F 2250/0042A61B 18/04A61B 2018/00601A61L 2400/16
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Claims

Abstract

Medical devices utilizing shape memory alloys and associated methods are disclosed herein. One aspect of the present technology, for example, is directed toward a treatment element configured to be positioned within a body lumen and coupled to an energy source. At least a portion of the treatment element may be made of a shape memory alloy, and wherein application of thermal energy to the treatment element from the energy source transforms the treatment element from the martensitic state to the austenitic state in which the treatment element is configured to cut, ablate, resect, and/or cauterize tissue.

Claims

exact text as granted — not AI-modified
I/we claim: 
     
         1 . A device for removing tissue from a body lumen, the device comprising:
 a delivery shaft having a lumen therethrough;   an energy source;   a manipulation member configured to be slidably received through the lumen of the delivery shaft, wherein the manipulation member has a distal portion configured to be positioned within the body lumen; and   a treatment element at the distal portion of the manipulation member and coupled to the energy source, at least a portion of the treatment element made of a shape memory alloy and having a low-profile martensitic state for delivery through the elongated shaft and an expanded, austenitic state that forms a pre-set shape having a cross-sectional dimension that is greater than the cross-sectional dimension of the shaft, and   wherein application of thermal energy to the treatment element from the energy source transforms the treatment element from the martensitic state to the austenitic state, and   wherein, when the treatment element is in the austenitic state, the treatment element is configured to cut, ablate, resect, and/or cauterize tissue.   
     
     
         2 . The device of  claim 1 , wherein the treatment element transforms from the martensitic state to the austenitic state at a temperature above 40 degrees Celsius. 
     
     
         3 . The device of  claim 1 , wherein the energy source is configured to deliver radiofrequency energy to the treatment element. 
     
     
         4 . The device of  claim 3 , wherein the treatment element is thermally activated and transforms from the martensitic state at a frequency of from about 100 kHz to about 5 MHz. 
     
     
         5 . The device of  claim 1 , wherein the distal portion of the manipulation member is configured to be delivered to a uterine cavity. 
     
     
         6 . The device of  claim 5 , wherein the device is configured to separate a tumor from the uterine cavity. 
     
     
         7 . The device of  claim 1 , wherein the treatment element has a single loop configuration. 
     
     
         8 . The device of  claim 1 , wherein the treatment element has a multiple loop configuration. 
     
     
         9 . The device of  claim 1 , wherein the delivery shaft is a portion of a hysteroscopic resectoscope. 
     
     
         10 . The device of  claim 1 , wherein the lumen of the delivery shaft includes a fluid medium. 
     
     
         11 . The device of  claim 1 , wherein a cross-sectional dimension of the delivery shaft is no greater than 8 mm. 
     
     
         12 . The device of  claim 1 , wherein the tissue is at least one of a leiomyoma and endometrium. 
     
     
         13 . A device for removing tissue from a body lumen, the device comprising:
 a delivery shaft having a lumen therethrough;   an energy source;   a manipulation member configured to be slidably received through the lumen of the delivery shaft, wherein the manipulation member has a distal portion configured to be positioned within the body lumen; and   a treatment element at the distal portion of the manipulation member and coupled to the energy source, at least a portion of the electrode made of a shape memory alloy and having a low-profile martensitic state for delivery through the elongated shaft and an expanded, austenitic state that forms a pre-set shape having a cross-sectional dimension that is greater than the cross-sectional dimension of the shaft, and   wherein application of ultrasonic energy to the treatment element from the energy source transforms the treatment element from the martensitic state to the austenitic state, and   wherein, when the treatment element is in the austenitic state, the electrode is configured to cut, ablate, resect, morcellate, and/or cauterize tissue.   
     
     
         14 . The device of  claim 13 , wherein the treatment element transforms from the martensitic state to the austenitic state at a frequency of from about 27 kHz to about 75 kHz. 
     
     
         15 . The device of  claim 13 , wherein the energy source is configured to deliver ultrasonic energy to the treatment element. 
     
     
         16 . The device of  claim 13 , wherein the treatment element is generally straight in a martensitic state and bent in an austenitic state. 
     
     
         17 . The device of  claim 13 , wherein the distal portion of the manipulation member is configured to be delivered to a uterine cavity. 
     
     
         18 . The device of  claim 17 , wherein the device is configured to separate a tumor from the uterine cavity. 
     
     
         19 . The device of  claim 13 , wherein the treatment element has a single loop configuration. 
     
     
         20 . The device of  claim 13 , wherein the treatment element has a multiple loop configuration. 
     
     
         21 . The device of  claim 13 , wherein the delivery shaft is a portion of a hysteroscopic resectoscope. 
     
     
         22 . The device of  claim 13 , wherein the lumen of the delivery shaft includes a fluid medium. 
     
     
         23 . The device of  claim 13 , wherein a cross-sectional dimension of the delivery shaft is no greater than 3 mm. 
     
     
         24 . The device of  claim 13 , wherein the tissue is at least one of a leiomyoma and endometrium.

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