Effect of Intense vs. Standard Hypertension Management on Nighttime Blood Pressure - an Ancillary Study to SPRINT

NACompletedINTERVENTIONAL
Enrollment

897

Participants

Timeline

Start Date

June 30, 2013

Primary Completion Date

June 30, 2017

Study Completion Date

July 31, 2017

Conditions
Hypertension
Interventions
OTHER

Intensive BP Arm

Participants in the Intensive arm have a goal of SBP \<120 mmHg.

OTHER

Standard BP arm

Participants in the Standard BP arm have a goal of SBP \<140 mmHg.

Trial Locations (10)

19104

University of Pennsylvania, Philadelphia

20422

Washington DC VA Medical Center, Washington D.C.

28203

Carolinas Medical Center, Charlotte

32224

Mayo Clinic, Jacksonville

35294

University of Alabama Birmingham, Birmingham

37235

Vanderbilt University, Nashville

38104

Memphis VA, Memphis

44129

Louis Stokes Cleveland VA Medical Center, Cleveland

77030

Houston VA, Houston

84112

University of Utah, Salt Lake City

Sponsors
All Listed Sponsors
collaborator

Wake Forest University

OTHER

collaborator

Louis Stokes VA Medical Center

FED

collaborator

University of Pennsylvania

OTHER

collaborator

Carolinas Medical Center

OTHER

collaborator

Mayo Clinic

OTHER

collaborator

University of Utah

OTHER

collaborator

Vanderbilt University

OTHER

collaborator

University of Alabama at Birmingham

OTHER

collaborator

Michael E. DeBakey VA Medical Center

FED

collaborator

Memphis VA Medical Center

FED

collaborator

Washington D.C. Veterans Affairs Medical Center

FED

lead

University of Minnesota

OTHER

NCT01835249 - Effect of Intense vs. Standard Hypertension Management on Nighttime Blood Pressure - an Ancillary Study to SPRINT | Biotech Hunter | Biotech Hunter