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RECRUITING

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

NCT06895590 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 205 participants
Start Date 2025-10-02
Est. Completion 2026-02

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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. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 186 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Non-cardiac Surgical appearing as the primary indexed condition, and to 1 intervention — of which Philips Advanced Monitoring Cuff (i.e. AMC) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06895590 reports 4 study locations spanning 3 distinct geographic areas — top geographies include North Carolina, Massachusetts, Bavaria. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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: Non-cardiac Surgical, Intensive Care Unit (ICU). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06895590?

The interventions under investigation include: Philips Advanced Monitoring Cuff (i.e. AMC) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06895590?

This trial is sponsored by Philips Clinical & Medical Affairs Global, which has 186 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial