NIBP Validation Study

RecruitingOBSERVATIONAL
Enrollment

189

Participants

Timeline

Start Date

June 23, 2023

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Critical Illness
Interventions
DEVICE

Philips IntelliVue X3 Patient Monitor

All subjects enrolled in this study will receive one Philips non-invasive blood pressure cuff. This cuff will be connected via compatible hose to the Philips IntelliVue X3 monitor hosting the released or investigational NIBP algorithm. The invasive blood pressure from the radial arterial line will also be connected to the Philips IntelliVue X3 monitor. The Philips IntelliVue X3 monitor will in turn be connected to a laptop for data collection.

Trial Locations (5)

27157

NOT_YET_RECRUITING

Wake Forest University Health Sciences, Winston-Salem

29425

NOT_YET_RECRUITING

Medical University of South Carolina, Charleston

32224

COMPLETED

Mayo Clinic Jacksonville, Jacksonville

84112

RECRUITING

University of Utah, Salt Lake City

97239

NOT_YET_RECRUITING

Oregon Health & Science University, Portland

All Listed Sponsors
lead

Philips Clinical & Medical Affairs Global

INDUSTRY

NCT05673408 - NIBP Validation Study | Biotech Hunter | Biotech Hunter