NIBP Validation Study
Recruiting · NCT05673408
Conditions: Critical Illness
At a glance
- Research payments reported, 2025
- $99,082
- U.S. investigators named
- 3
- Sites paid
- 3
- Planned or actual enrollment
- 189
About the trial
- Sponsor
- Philips Clinical & Medical Affairs Global
- Tested
- Philips IntelliVue X3 Patient Monitor (device)
- Dates
- Started 2023-06-23; completion 2027-03-31
- Results posted
- Not yet
The purpose of this study is to compare measurements of blood pressure (BP) between the Philips non-invasive blood pressure (NIBP) system (including NIBP cuff and portable patient monitor) and invasive radial for Subject Group 2 and 3, and radial or umbilical arterial line for neonates (A-line) in critical care patients.
From ClinicalTrials.gov, last updated 2026-05-26. Full record, eligibility and contacts (opens in a new tab)
Industry funding
Philips North America LLC reported $99,082 in research payments for this study in 2025 (5 payments).
Products named: Nibp Reusable Cuffs
Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.
U.S. investigators named on this study
- Monica M. Rabanal, NP Nurse Practitioners · Evergreen, CO
- Ashish K. Khanna, M.D. Critical Care Medicine · Winston Salem, NC
- Amy R. Quinn, M.D. Neonatology · San Antonio, TX
Clinicians the company named as principal investigators in its Open Payments reports.
Sites paid to run it
- Element Materials Technology $82,197
- University of Texas Health Science Center at San Antonio $15,345
- Wake Forest University Health Sciences $1,540
Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.