Fresenius Noninvasive Blood Pressure Validation

NACompletedINTERVENTIONAL
Enrollment

159

Participants

Timeline

Start Date

September 17, 2020

Primary Completion Date

December 4, 2020

Study Completion Date

December 4, 2020

Conditions
Blood Pressure
Interventions
DEVICE

Blood Pressure Measurement

The purpose of this study is to provide supporting documentation for Noninvasive blood pressure measurement accuracy claims for Fresenius 5008S BPM Module and Cuffs on the intended population(s). The same arm sequential method with dual observer auscultation will be used to collect data.

Trial Locations (1)

80027

Clinimark, Site ID#001, Louisville

All Listed Sponsors
lead

Fresenius Medical Care North America

INDUSTRY

NCT04573595 - Fresenius Noninvasive Blood Pressure Validation | Biotech Hunter | Biotech Hunter