IP Library Granted Patent US 9,078,801
Granted Patent B2
US 9,078,801 · App. 13/784,573 · Granted Jul 14, 2015

Implantable electroacupuncture device and method for treating erectile dysfunction

Inventors: Jeffrey H. Greiner (Valencia, CA); David K. L. Peterson (Valencia, CA); Chuladatta Thenuwara (Castaic, CA); Stacy O. Greiner (Valenica, CA)
Assignee: Valencia Technologies Corporation
A61H39/002A61N1/36107A61N1/36175A61N1/3756A61N1/37205A61N1/18A61N1/362A61N1/36125A61N1/36153A61N1/36157A61N1/375A61N1/3758A61N1/3782Y10T29/49002
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Quick Facts
Patent No.
US 9,078,801
App. No.
13/784,573
Granted
Jul 14, 2015
Kind
B2
Abstract

An implantable electroacupuncture device (IEAD) treats an erectile dysfunction condition of a patient through application of stimulation pulses applied at a target tissue location underlying, or in the vicinity of, at least one of acupoints BL52, BL23 or GV4. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years.

Claims (10)

1. A method for treating erectile dysfunction in a patient comprising the steps of:

(a) implanting a thin, self-contained, leadless, coin-sized electroacupuncture (EA) device in the patient below the patient's skin at at least one specified stimulation site;

(b) enabling the EA device to generate stimulation sessions at a duty cycle that is less than 0.05, each stimulation session comprising a series of stimulation pulses, wherein the duty cycle is the ratio of T3/T4, where T3 is the time or duration of each stimulation session, and T3 is at least 10 minutes, and T4 is the time between stimulation sessions, and T4 is at least 1440 minutes [1 day] and no more than 20,160 minutes [14 days], thereby applying a stimulation regimen that limits the frequency and duration of the stimulation sessions; and

(c) continuously delivering the stimulation pulses of each stimulation session to the at least one specified stimulation site through at least two concentric electrodes/arrays configured on an outside surface of the thin, self-contained, leadless, coin-sized EA device, wherein the continuous delivery of the stimulation regimen, as limited by requiring the T3/T4 ratio to always be less than 0.05, slowly and methodically remodels the patient's central nervous system to produce a sustained therapeutic benefit of the patient's erectile dysfunction condition.

2. The method of treating erectile dysfunction of claim 1 wherein the at least one specified stimulation site at which the stimulation pulses are applied comprises tissue underlying, or in the immediate vicinity of, at least one of acupoints BL52, BL23 or GV4.

3. The method of treating erectile dysfunction of claim 2 further comprising configuring the at least two concentric electrodes/arrays on the outside surface of the EA device as one central electrode/array, and as one annular electrode/array that surrounds the central electrode/array, wherein the spacing between the center of the central electrode/array and an edge of the annular electrode/array closest to the central electrode/array comprises at least 5 mm.

4. The method of treating erectile dysfunction of claim 3 further including forming the annular electrode/array as a ring electrode/array attached around a perimeter edge of the coin-sized EA device.

5. The method of treating erectile dysfunction of claim 4 further including configuring the central electrode/array as a cathode electrode and the perimeter-edge ring electrode/array as an anode electrode.

6. The method of treating erectile dysfunction of claim 2 wherein enabling the EA device to generate stimulation sessions includes generating the series of stimulation pulses within each stimulation session so that each stimulation pulse has a duration of between 0.1 and 2.0 milliseconds, occurs at a rate of between 1 and 15 Hz and has a reverse trapezoidal wave shape.

7. The method of treating erectile dysfunction of claim 6 further comprising setting T3, the duration of the stimulation session, to a value between 10 minutes and 30 minutes.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded May 6, 2026
From: MEDTRONIC, INC.
To: VALENCIA BIOSCIENCE, INC.
Reel/Frame 075721/0223 →
SECURITY INTEREST Recorded Oct 27, 2023
From: VALENCIA BIOSCIENCE, INC.
To: MEDTRONIC, INC.
Reel/Frame 065382/0738 →
SECURITY INTEREST Recorded Aug 4, 2021
From: VALENCIA BIOSCIENCE, INC.
To: MEDTRONIC, INC.
Reel/Frame 057088/0352 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 3, 2020
From: VALENCIA TECHNOLOGIES CORPORATION
To: VALENCIA BIOSCIENCE, INC.
Reel/Frame 053684/0656 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2015
From: GREINER, JEFFREY H; PETERSON, DAVID K.L.; THENUWARA, CHULADATTA; CHAMBLISS, STACY GREINER
To: VALENCIA TECHNOLOGIES CORPORATION
Reel/Frame 034941/0317 →
Continuity (9)
Continuation In Part 13598582 · Aug 29, 2012
Provisional Application 61609875 · Mar 12, 2012
Provisional Application 61672257 · Jul 16, 2012
Provisional Application 61672661 · Jul 17, 2012
Provisional Application 61673254 · Jul 19, 2012
Provisional Application 61674691 · Jul 23, 2012
Provisional Application 61676275 · Jul 26, 2012
Provisional Application 61606995 · Mar 6, 2012
Related Publication 20140214112A1 · Jul 31, 2014