Systems and methods of neuromodulation stimulation for the restoration of sexual function

• US 8,805,533 B2
• Filed: 02/21/2011
• Issued: 08/12/2014
• Est. Priority Date: 06/10/2004
• Status: Expired due to Fees

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Boggs, Joseph W. II, Thrope, Geoffrey B., Strother, Robert B., Mrva, Joseph J.
• Primary Examiner(s): BEHRINGER, LUTHER G
• Application Number:
  US13/031,482
• Publication Number:
  US 20110144468A1
• Time in Patent Office: 1,268 Days
• Field of Search: 607116-119, 607/137
• US Class Current: 607/116
• CPC Class Codes: A61M 2205/054 with electrotherapy
• CPC Class Codes: A61M 2210/1067 Anus
• CPC Class Codes: A61M 2210/1089 Urethra
• CPC Class Codes: A61N 1/05 for implantation or insertion into the body, e.g. heart electrode A61N1/06 takes precedence
• CPC Class Codes: A61N 1/0512 Anal electrodes
• CPC Class Codes: A61N 1/0524 Vaginal electrodes
• CPC Class Codes: A61N 1/36007 of urogenital or gastrointestinal organs, e.g. for incontinence control
• CPC Class Codes: A61N 1/36107 Sexual dysfunction stimulating genital organs A61N1/36007

Abstract

Systems and methods use an external and/or implantable pulse generator system for neuromodulation stimulation to treat sexual dysfunction by the unilateral or bilateral stimulation of a target nerve A and/or a target nerve B using one or more leads and electrodes implanted in tissue in the pelvic region. The electrical stimulation waveform may be conveyed to the target nerve A electrode for a first predetermined amount of time, and conveyed to the target nerve B electrode for a second predetermined amount of time.

Claims

1. A stimulating catheter system comprising a catheter, the catheter comprising:

an elongated flexible body having a proximal end and a distal end and at least one lumen extending at least a portion of the body;

an inflatable balloon disposed at or near the distal end;

an electrode array disposed along the flexible body, wherein respective electrodes of the electrode array are regularly spaced along the flexible body; and

an electrical lead coupled to each electrode in the electrode array and extending through the body, wherein the electrical lead is configured to be connected to an electrical source via an external connection,

wherein the catheter is configured to deliver neuromodulation stimulation to a patient from the electrical source via the electrical lead and the electrode array,

wherein the at least one lumen includes a first, and

wherein the first lumen exits the flexible body at or near the distal end and serves as a path for fluid flow in and out of the flexible body at or near the distal end.

2. The catheter system according to claim 1,

wherein the electrode array is disposed proximal to the inflatable balloon along the flexible body.

3. The catheter system according to claim 1,

wherein the flexible body is configured to be positioned within the urethra of a male and/or female animal or human.

4. The catheter system according to claim 1,

wherein the flexible body is configured to be positioned within the rectum of a male and/or female animal or human.

5. The catheter system according to claim 1,

wherein the flexible body is configured to be positioned within the vagina of a female animal or human.

6. The catheter system according to claim 1,

wherein at least one electrode is positioned on or near the distal tip of the flexible body.

7. The catheter system according to claim 1,

wherein the electrode array is coupled to the outside of the flexible body.

8. The catheter system according to claim 1,

wherein the flexible body is malleable.

9. The catheter system according to claim 1,

wherein the flexible body is adapted to be bendable while positioned within a body cavity, and is configured to be bendable during removal without causing damage to the body cavity or internal structures.

10. The catheter system according to claim 1,

wherein the flexible body is pre-bent in a desired configuration so as to maintain its shape during insertion and stimulation.

11. The catheter system according to claim 1,

wherein the electrode array comprises a proximal portion and a distal portion, the electrodes of the proximal portion are spaced apart a first distance, and the electrodes of the distal portion are spaced apart at a second distance less than the first distance.

12. The catheter system according to claim 1,

wherein the electrode array comprises a proximal portion and a distal portion, the electrodes of the proximal portion are spaced about 1 cm to about 5 cm apart, and the electrodes of the distal portion are spaced apart about 0.1 mm to about 2 cm apart.

13. The catheter system according to claim 1,

wherein the electrode array comprises a proximal portion and a distal portion, the electrodes of the proximal portion are spaced about 1.5 cm to 2 cm apart, and the electrodes of the distal portion are spaced apart about 0.3 cm to about 0.7 cm apart.

14. The catheter system according to claim 1,

wherein the flexible body includes a coude tip at the distal end.

15. The catheter system according to claim 1, wherein the at least one lumen comprises a second lumen extending at least a portion of the catheter body.

16. The catheter system according to claim 15,

wherein the second lumen carries the electrical lead to the electrode array.

17. The catheter system according to claim 15,

wherein the second lumen is in fluid flow communication with the balloon and serves as a path for fluid flow to fill and drain the balloon.

18. The catheter system according to claim 15,

wherein the at least one lumen includes a third lumen.

19. The catheter system according to claim 18,

wherein the third lumen is in fluid flow communication with the balloon and serves as a path for fluid flow to fill and drain the balloon.

20. The catheter system according to claim 1,

wherein the electrode array is configured to deliver the neuromodulation therapy in a monopolar, bipolar, and/or multi-polar configuration.

21. The catheter system according to claim 1,

wherein the neuromodulation stimulation therapy delivered via the electrode array is configured to cause efferent and/or afferent stimulation of at least one of a target nerve A and a target nerve B, to produce an erection.

22. The catheter system according to claim 21, wherein the target nerve A is selected from the group consisting of the cavernous nerve and/or spinal, sacral, lumbar, and/or thoracic roots and/or branches;

the prostatic plexus and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches;

the pelvic nerve and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches;

the hypogastric nerve and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches; and

the splanchnic nerve and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches, and

wherein the target nerve B is selected from the group consisting of the pudendal nerve and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches;

the perineal nerve and/or its spinal, sacral, lumbar, and/or thoracic roots and/or branches;

the nerves that innervate the ischiocavernosus, bulbocavernosus, and/or bulbospongiosus muscles and/or their spinal, sacral, lumbar, and/or thoracic roots and/or branches; and

the nerves that innervate the transverse perineal muscles and/or their spinal, sacral, lumbar, and/or thoracic roots and/or branches.

23. The catheter system of claim 1, further comprising the electrical source configured to be connected to the electrical lead via the external connection, wherein the electrical source comprises a neuromodulation stimulation generator configured to generate the neuromodulation stimulation delivered to the patient.

24. The catheter system according to claim 23,

wherein the neuromodulation stimulation delivered via the electrode array is configured to cause afferent stimulation of at least one of a target nerve A and a target nerve B, the afferent stimulation activating central nervous system circuitry that coordinates and/or produces efferent activity in at least one of the target nerve A and the target nerve B, to produce an erection.

25. The catheter system according to claim 23,

wherein the neuromodulation stimulation delivered via the electrode array is configured to cause afferent stimulation of the dorsal genital nerves and/or its roots and/or its branches, the afferent stimulation activating central nervous system circuitry that coordinates and/or produces efferent activity in at least one of a target nerve A and a target nerve B, to produce an erection.

26. The catheter system of claim 1, wherein the at least one lumen includes a second lumen, wherein the second lumen carries the electrical lead to the electrode array, is in fluid flow communication with the balloon, and serves as a path for fluid flow to fill and drain the balloon.