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

Conditions

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

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Philips Advanced Monitoring Cuff (i.e. AMC) — DEVICE
  Investigational, non-invasive upper arm cuff

Study Details

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.

Key Dates

Start date

Oct 2, 2025

Status verified

Feb 2026

Primary completion

Feb 28, 2026

Completion

Feb 28, 2026

Study Design

Enrollment

205 participants (estimated)

Arms

• Arm: Philips AMC Cuff
  This is a non-randomized, single arm, self-controlled observational study. The Philips AMC cuff will be tested on all enrolled participants.

Primary Outcome Measure

Primary Endpoints [ Time Frame: Approximately 8 months accrual and follow-up evaluation period. ]

Central Contacts

• Lea Egger
  +49 1722314318
  [email protected]

Locations (3)

Find similar trials in Boston, MA