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RECRUITING

Real World Effectiveness of the Cordella Pulmonary Artery Sensor System in Patients With Chronic Heart Heart Failure

NCT06783335 · View on ClinicalTrials.gov ↗

Study Summary

This retrospective, non-randomized cohort study will evaluate how well the Cordella PA Sensor System works compared to standard medication treatment in people with chronic heart failure. The study will track patients for two years to see if those using the Cordella system have fewer deaths and hospitalizations related to heart failure.

Interventions

  • DEVICE Cordella PA Sensor System
  • DRUG Standard of Care Pharmacologic Therapy

Study Locations (1)

Illinois

  • Endotronix — Naperville

Trial Details

FieldValue
Enrollment Target 2,150 participants
Start Date 2025-02-07
Est. Completion 2030-12-31

Sponsor

Endotronix

34 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06783335

The ClinicalTrials.gov registry entry for NCT06783335 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 2,150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endotronix, which has 34 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 Heart Failure appearing as the primary indexed condition, and to 2 interventions — of which Cordella PA Sensor System 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: NCT06783335 reports 1 study location spanning 1 distinct geographic area — top geographies include 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 NCT06783335 about?

NCT06783335 is a clinical study titled "Real World Effectiveness of the Cordella Pulmonary Artery Sensor System in Patients With Chronic Heart Heart Failure". This retrospective, non-randomized cohort study will evaluate how well the Cordella PA Sensor System works compared to standard medication treatment in people with chronic heart failure. The study will track patients for two years to see if those using the Cordella system have fewer deaths and hospi...

What is the current status of trial NCT06783335?

This trial is currently recruiting. The enrollment target is 2,150 participants. The study started on 2025-02-07. Estimated completion is 2030-12-31.

What conditions does trial NCT06783335 study?

This clinical trial studies the following conditions: Heart Failure, Heart Failure NYHA Class III. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06783335?

The interventions under investigation include: Cordella PA Sensor System (DEVICE), Standard of Care Pharmacologic Therapy (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06783335?

This trial is sponsored by Endotronix, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06783335 being conducted?

This trial has 1 study location across Illinois. 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