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NCT06895590 · ClinicalTrials.gov registry record
The HIgh-fidelity Hydraulic couPling Upper-arm Cuff Assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial
A clinical trial of Intensive Care Unit (ICU) and Non-cardiac Surgical, sponsored by Philips Clinical & Medical Affairs Global.
- Recruiting
- Registry status
- 205
- Enrollment target
- 4
- Study locations
NCT06895590 is a study of Intensive Care Unit (ICU) and Non-cardiac Surgical that is actively recruiting participants, run by Philips Clinical & Medical Affairs Global. The registered enrollment target is 205 participants. The trial reports 4 study locations across 3 states.
The verdict
NCT06895590, a study of Intensive Care Unit (ICU) and Non-cardiac Surgical, is actively recruiting participants, sponsored by Philips Clinical & Medical Affairs Global.
- RECRUITING
- Registry status
- 205 participants
- Enrollment target
- 4
- Study locations
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 Studied
Interventions
- DEVICE Philips Advanced Monitoring Cuff (i.e. AMC)
Study Locations (4)
North Carolina
- Duke University Health System - Durham
- Wake Forest Baptist Medical Center - Winston-Salem
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Bavaria
- LMU Klinikum , Campus Großhadern - München
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 205 participants |
| Start Date | 2025-10-02 |
| Est. Completion | 2026-02 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06895590
The ClinicalTrials.gov registry entry for NCT06895590 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 205 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Philips Clinical & Medical Affairs Global, which has 45 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Intensive Care Unit (ICU) appearing as the primary indexed condition, and to 1 intervention - of which Philips Advanced Monitoring Cuff (i.e. AMC) is the first listed.
NCT06895590 reports 4 study locations spanning 3 distinct geographic areas - top geographies include North Carolina, Massachusetts, Bavaria.
Frequently Asked Questions
What is clinical trial NCT06895590 about?
NCT06895590 is a clinical study titled "The HIgh-fidelity Hydraulic couPling Upper-arm Cuff Assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial". 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.
What is the current status of trial NCT06895590?
This trial is currently recruiting. The enrollment target is 205 participants. The study started on 2025-10-02. Estimated completion is 2026-02.
What conditions does trial NCT06895590 study?
This clinical trial studies the following conditions: Intensive Care Unit (ICU), Non-cardiac Surgical.
What interventions are being tested in trial NCT06895590?
The interventions under investigation include: Philips Advanced Monitoring Cuff (i.e. AMC) (DEVICE).
Who is sponsoring clinical trial NCT06895590?
This trial is sponsored by Philips Clinical & Medical Affairs Global, which has 45 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06895590 being conducted?
This trial has 4 study locations across Massachusetts, North Carolina, Bavaria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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