IP Library Granted Patent US 11,400,278
Granted Patent B2
US 11,400,278 · App. 16/693,008 · Granted Aug 2, 2022

Methods and systems for treating hypertension using an implantable stimulator

Inventors: Jeffrey H. Greiner (Valencia, CA); David K. L. Peterson (Valencia, CA); Chuladatta Thenuwara (Castaic, CA)
Assignee: Valencia Bioscience, Inc.
A61N1/0504A61H39/002A61N1/36117A61N1/36175A61N1/3756A61N1/37205A61H2201/5005A61H2201/5035A61H2201/5038A61H2201/5097A61N1/3605A61N1/36125A61N1/3758A61N1/3782Y10S128/907
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Quick Facts
Patent No.
US 11,400,278
App. No.
16/693,008
Granted
Aug 2, 2022
Kind
B2
Abstract

A method of treating hypertension in a patient includes generating, by an implantable stimulator configured to be implanted beneath a skin surface of the patient, stimulation sessions at a duty cycle that is less than 0.05 and applying, by the implantable stimulator in accordance with the duty cycle, the stimulation sessions to a tissue location associated with the hypertension. The duty cycle is a ratio of T 3 to T 4 . Each stimulation session included in the stimulation sessions has a duration of T 3 minutes and occurs at a rate of once every T 4 minutes. The implantable stimulator is powered by a primary battery located within the implantable stimulator and having an internal impedance greater than 5 ohms.

Claims (42)

1. A method of treating hypertension in a patient, comprising:

generating, by an implantable stimulator configured to be implanted beneath a skin surface of the patient, stimulation sessions at a duty cycle that is less than 0.05, wherein

the duty cycle is a ratio of T 3 to T 4 ,

each stimulation session included in the stimulation sessions has a duration of T 3 minutes and occurs at a rate of once every T 4 minutes, and

the implantable stimulator is powered by a primary battery located within the implantable stimulator and having an internal impedance greater than 5 ohms; and

applying, by the implantable stimulator in accordance with the duty cycle, the stimulation sessions to a tissue location associated with the hypertension.

2. The method of claim 1 , wherein the tissue location comprises a median nerve of the patient.

3. The method of claim 1 , wherein the implantable stimulator is configured to be implanted at an acupoint comprising at least one of PC5, PC6, ST36, and ST37.

4. The method of claim 1 , wherein T 3 is at least 10 minutes and less than 40 minutes, and wherein T 4 is at least 1440 minutes.

5. The method of claim 1 , further comprising:

receiving, by the implantable stimulator from a device external to the implantable stimulator, a control command that sets the times T 3 and T 4 to appropriate values configured to treat the hypertension;

wherein the generating of the stimulation sessions is performed in accordance with the control command.

6. The method of claim 5 , wherein the receiving of the control command comprises detecting, with an electromagnetic field sensor included in the implantable stimulator, a magnetic field generated by the device external to the implantable stimulator.

7. The method of claim 1 , wherein the primary battery located within the implantable stimulator has a capacity of less than 60 milliamp-hours (mAh).

8. The method of claim 1 , wherein the primary battery located within the implantable stimulator is a coin-cell battery.

9. The method of claim 1 , wherein the applying of the stimulation sessions to the tissue location comprises applying the stimulation sessions to the tissue location by way of an electrode array.

10. The method of claim 9 , wherein the electrode array comprises a central electrode of a first polarity centrally located on a first surface of a housing of the implantable stimulator and an annular electrode of a second polarity and that is spaced apart from the central electrode.

11. The method of claim 10 , wherein the annular electrode is located on the first surface of the housing.

12. The method of claim 10 , wherein the annular electrode comprises a ring electrode located around a perimeter edge of the housing.

13. The method of claim 9 , wherein the electrode array comprises a plurality of electrodes located on a lead that is attached to the implantable stimulator.

14. An implantable stimulator for treating hypertension in a patient, comprising:

a housing configured to be implanted beneath a skin surface of the patient,

pulse generation circuitry located within the housing, wherein the pulse generation circuitry is configured to

generate stimulation sessions at a duty cycle that is less than 0.05, and

apply, in accordance with the duty cycle, the stimulation sessions a tissue location associated with the hypertension; and

a primary battery located within the housing and having an internal impedance greater than 5 ohms, the primary battery configured to provide operating power to the pulse generation circuitry;

wherein

the duty cycle is a ratio of T 3 to T 4 , and

each stimulation session included in the stimulation sessions has a duration of T 3 minutes and occurs at a rate of once every T 4 minutes.

15. The implantable stimulator of claim 14 , wherein the tissue location comprises a median nerve of the patient.

16. The implantable stimulator of claim 14 , wherein the primary battery located within the implantable stimulator has a capacity of less than 60 milliamp-hours (mAh).

17. The implantable stimulator of claim 14 , wherein the primary battery located within the implantable stimulator is a coin-cell battery.

18. The implantable stimulator of claim 14 , further comprising an electrode array, wherein the implantable stimulator is configured to apply the stimulation sessions to the tissue location comprises by way of the electrode array.

19. The implantable stimulator of claim 18 , wherein the electrode array comprises:

a central electrode of a first polarity centrally located on a surface of the housing; and

an annular electrode of a second polarity and that is spaced apart from the central electrode.

20. A system for treating hypertension in a patient, comprising:

means for generating, within an implantable stimulator configured to be implanted beneath a skin surface of the patient, stimulation sessions at a duty cycle that is less than 0.05, wherein

the duty cycle is a ratio of T 3 to T 4 ,

each stimulation session included in the stimulation sessions has a duration of T 3 minutes and occurs at a rate of once every T 4 minutes, and

the implantable stimulator is powered by a primary battery located within the implantable stimulator and having an internal impedance greater than 5 ohms; and

means for applying, in accordance with the duty cycle, the stimulation sessions to a tissue location associated with the hypertension.

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 Nov 22, 2019
From: GREINER, JEFFREY H.; PETERSON, DAVID K.L.; THENUWARA, CHULADATTA
To: VALENCIA TECHNOLOGIES CORPORATION
Reel/Frame 051092/0548 →
Continuity (12)
Continuation 15700013 · Sep 8, 2017
Division 14805355 · Jul 21, 2015
Continuation 14446500 · Jul 30, 2014
Division 13598575 · Aug 29, 2012
Provisional Application 61575869 · Aug 30, 2011
Provisional Application 61606995 · Mar 6, 2012
Provisional Application 61609875 · Mar 12, 2012
Provisional Application 61672257 · Jul 16, 2012
Provisional Application 61672661 · Jul 17, 2012
Provisional Application 61674691 · Jul 23, 2012
Provisional Application 61676275 · Jul 26, 2012
Related Publication 20200121917A1 · Apr 23, 2020