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RECRUITING

Pivotal Study for the Cardiac Performance System (CPS)

NCT06870591 · View on ClinicalTrials.gov ↗

Study Summary

This multi-center, observational study evaluates the accuracy of the Cardiac Performance System (CPS), a non-invasive device, for measuring hemodynamic parameters in adult patients undergoing clinically indicated right heart catheterization. The study compares CPS measurements to invasive measurements to assess agreement and potential clinical utility.

Conditions Studied

Interventions

  • DEVICE Cardiac Performance System (CPS)

Study Locations (10)

New Jersey

  • Hackensack University Medical Center — Hackensack
  • Jersey Shore University Medical Center — Neptune City

Alabama

  • Huntsville Hospital Heart Center — Huntsville

Illinois

  • Endeavor Health — Evanston

New York

  • Columbia University Irving Medical Center / NewYork-Presbyterian Hospital — New York

Ohio

  • The Ohio State University Medical Center — Columbus

Pennsylvania

  • University of Pennsylvania - Penn Presbyterian Medical Center — Philadelphia

South Carolina

  • Medical University of South Carolina — Charleston

Tennessee

  • The Stern Cardiovascular Foundation, Inc. / Baptist Memorial Hospital — Germantown

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2025-04-22
Est. Completion 2026-05-30

Sponsor

Sensydia Corporation

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06870591

The ClinicalTrials.gov registry entry for NCT06870591 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 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sensydia Corporation, which has 33 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Cardiovascular Diseases appearing as the primary indexed condition, and to 1 intervention — of which Cardiac Performance System (CPS) 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: NCT06870591 reports 10 study locations spanning 9 distinct geographic areas — top geographies include New Jersey, Alabama, Illinois. 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 NCT06870591 about?

NCT06870591 is a clinical study titled "Pivotal Study for the Cardiac Performance System (CPS)". This multi-center, observational study evaluates the accuracy of the Cardiac Performance System (CPS), a non-invasive device, for measuring hemodynamic parameters in adult patients undergoing clinically indicated right heart catheterization. The study compares CPS measurements to invasive measuremen...

What is the current status of trial NCT06870591?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2025-04-22. Estimated completion is 2026-05-30.

What conditions does trial NCT06870591 study?

This clinical trial studies the following conditions: Cardiovascular Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06870591?

The interventions under investigation include: Cardiac Performance System (CPS) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06870591?

This trial is sponsored by Sensydia Corporation, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06870591 being conducted?

This trial has 10 study locations across Alabama, Illinois, New Jersey, New York, Ohio. 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