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

NCT06895590 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 205

Last updated 2026-02-27

No results posted yet for this study

Summary

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.

Conditions

  • Non-cardiac Surgical
  • Intensive Care Unit (ICU)

Interventions

DEVICE

Philips Advanced Monitoring Cuff (i.e. AMC)

Investigational, non-invasive upper arm cuff

Sponsors & Collaborators

  • Philips Clinical & Medical Affairs Global

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-02
Primary Completion
2026-02-28
Completion
2026-02-28
FDA Device
Yes

Countries

  • United States
  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06895590 on ClinicalTrials.gov