BAROSTIM NEO Hypertension Pivotal Trial

NASuspendedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

April 12, 2013

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2026

Conditions
Uncontrolled Hypertension
Interventions
DEVICE

BAROSTIM NEO System and Medical Management

"Experimental: Device and Medical Management~Subjects have been implanted with the BAROSTIM NEO System and receive optimal medical management, including drugs to be determined by the subject's physician. Drug types include: Loop Diuretics; Thiazide Diuretics; Potassium-sparing Diuretics; Aldosterone receptor blockers; Beta-blockers; Beta-blockers with intrinsic sympathomimetic activity; Combined alpha- and beta-blockers; ACE inhibitors; Angiotensin II antagonists; Calcium channel blockers- non-Dihydropyridines; Calcium channel blockers- Dihydropyridines; Alpha1-blockers; Central alpha2-agonists and other centrally acting drugs; Direct vasodilators."

Trial Locations (11)

15212

Allegheny General Hospital, Pittsburgh

20037

George Washington University, Washington D.C.

32803

Florida Hospital, Orlando

33606

Tampa General Hospital, Tampa

48601

Michigan CardioVascular Institute, Saginaw

49770

Cardiac and Vascular Research Center of Northern Michigan, Petoskey

54401

Aspirus Wausau Hospital, Wausau

70360

Cardiovascular Institute of the South, Houma

85006

Arizona Heart Rhythm Research Center, Phoenix

89102

University Medical Center of Southern Nevada, Las Vegas

90033

University of Southern California, Los Angeles

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CVRx, Inc.

INDUSTRY

NCT01679132 - BAROSTIM NEO Hypertension Pivotal Trial | Biotech Hunter | Biotech Hunter