Validation Study in Patients of a Non-invasive Blood Pressure Monitor for Perioperative Use

UnknownOBSERVATIONAL
Enrollment

100

Participants

Timeline

Start Date

March 1, 2017

Primary Completion Date

December 30, 2019

Study Completion Date

December 30, 2019

Conditions
Intraoperative Hypotension
Interventions
DEVICE

ClearSight feasibility testing

A cuff is placed on a finger of the patient. The ClearSight system uses a volume clamp technology allowing measuring of continuous blood pressure waveform. Note: There will only be observational recordings, no interventions

Trial Locations (1)

1105AZ

RECRUITING

Academic Medical Center, Amsterdam

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Edwards Lifesciences

INDUSTRY

lead

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

OTHER