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RECRUITING
NCT06895603

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

Sponsor: Philips Clinical & Medical Affairs Global

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

75

Start Date

2025-10-28

Completion Date

2026-06

Last Updated

2026-02-27

Healthy Volunteers

No

Interventions

DEVICE

Philips Advanced Monitoring Cuff (AMC)

The Philips AMC is a Class II (USA) and Class IIb (EU) medical device that is a non-invasive, semirigid disposable upper arm cuff with an integrated pneumatic actuator enabling hydraulic coupling of tissue pressure waveforms from the upper arm tissue.

Locations (2)

UVA Health

Charlottesville, Virginia, United States

Universitätsklinikum Hamburg Eppendorf

Hamburg, Hamburg, Germany