The HIgh-fidelity Hydraulic couPling Upper-arm Cuff Assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial
Recruiting · NCT06895590
Conditions: Non-cardiac Surgical, Intensive Care Unit (ICU)
At a glance
- Research payments reported, 2025
- $41,250
- U.S. investigators named
- 2
- Sites paid
- 2
- Planned or actual enrollment
- 205
About the trial
- Sponsor
- Philips Clinical & Medical Affairs Global
- Tested
- Philips Advanced Monitoring Cuff (i.e. AMC) (device)
- Dates
- Started 2025-10-02; completion 2026-02
- Results posted
- Not yet
The purpose of this study is to compare measurements of blood pressure (BP) and fluid responsiveness between the Philips AMC and invasive radial arterial line in surgical patients.
From ClinicalTrials.gov, last updated 2026-02-27. Full record, eligibility and contacts (opens in a new tab)
Industry funding
Philips North America LLC reported $41,250 in research payments for this study in 2025 (3 payments).
Products named: Spo2 Adapter Cables
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
Clinicians the company named as principal investigators in its Open Payments reports.
Sites paid to run it
- Beth Israel Deaconess Medical Center, MA $21,500
- Duke University $19,750
Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.