Clinical Trial

The HIgh-fidelity Hydraulic couPling Upper-arm Cuff Assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial (Cardiac Output Study)

Study acronym: CO
Recruiting
View on ClinicalTrials.gov →
Summary
The purpose of this study is to compare cardiac output (CO), fluid responsiveness, and related measurements between the Philips AMC and PAC (Swan-Ganz) in ICU or surgical patients.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-03-19; most recent amendment 2026-02-24.
Status change: Not Yet Recruiting → Recruiting 2025-12-03
Trial Details
NCT Number NCT06895603
Lead Sponsor Philips Clinical & Medical Affairs Global
Conditions ICU, Pulmonary Artery Catheter (PAC), Swan-Ganz Catheter
Enrollment 75 participants
Start Date 2025-10-28
Primary Completion 2026-02 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2026-02-27