Clinical trial

PROACTIVE-HF IDE Trial Heart Failure NYHA Class III

NCT04089059 · Endotronix, Inc., Industry · Active, not recruiting

Key facts

NCT number NCT04089059
Title PROACTIVE-HF IDE Trial Heart Failure NYHA Class III
Official title A Prospective, Multi-Center, Open Label, Single Arm Clinical Trial Evaluating the Safety and Efficacy of the Cordella™ Pulmonary Artery Sensor System in NYHA Class III Heart Failure Patients (PROACTIVE- HF Trial)
Acronym PROACTIVE-HF
Lead sponsor Endotronix, Inc., Industry
Status Active, not recruiting
Study type Interventional
Conditions Heart Failure NYHA Class III
Intervention type Device
Interventions Cordella™ Pulmonary Artery Sensor System
Enrollment 738
Start date Jan 10, 2020
Primary completion Apr 1, 2028
Completion Apr 1, 2028
First posted Sep 13, 2019
Last update posted Mar 3, 2025
Countries Belgium, Ireland, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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