Fluid Responsiveness Evaluation in Sepsis-associated Hypotension

NACompletedINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

March 31, 2019

Study Completion Date

March 13, 2019

Conditions
SepsisHypotension
Interventions
DEVICE

Treatment Starling SV monitor

A dynamic assessment of fluid responsiveness will be performed at every clinical decision point for the first 72 hours of study enrollment. Fluid responsiveness will be assessed using a passive leg raise (PLR) and Starling SV hemodynamic monitor to guide corresponding treatment.

Trial Locations (12)

10016

NYU School of Medicine, New York

11215

New York Presbyterian Brooklyn Methodist Hospital, New York

30303

Grady Memorial Hospital, Atlanta

37232

Vanderbilt University Medical Center, Nashville

43210

Ohio State University Hospital, Columbus

46202

Indiana University Methodist Hospital, Indianapolis

77030

Baylor College of Medicine, Houston

80204

Denver Health, Denver

94143

University of California San Francisco Medical Center, San Francisco

97239

Oregon Health and Science University, Portland

02903

Rhode Island Hospital, Providence

Unknown

Royal Surrey County Hospital, Guildford

Sponsors
All Listed Sponsors
lead

Cheetah Medical Inc.

INDUSTRY