NIBP Validation Study (NCT05673408)
Non-Invasive Blood Pressure Validation Study
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Mayo Clinic Jacksonville — Jacksonville, Florida
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (5 Sites)
- Mayo Clinic Jacksonville — Jacksonville, Florida
- Wake Forest University Health Sciences — Winston-Salem, North Carolina
- Oregon Health & Science University — Portland, Oregon
- University Health Women's and Children's Hospital — San Antonio, Texas
- University of Utah — Salt Lake City, Utah
📞 Contact the Study Coordinator
Phone: (210) 517-4405
Email: natalie.hernandez@philips.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.