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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)
Conditions
Interventions
Cordella™ Pulmonary Artery Sensor System
Locations
74
United States
Ascension St Vincent's
Birmingham, Alabama, United States
Huntsville Hospital
Huntsville, Alabama, United States
Phoenix Cardiovascular Research Group/Insight
Phoenix, Arizona, United States
Loma Linda University
Loma Linda, California, United States
Eisenhower Medical Center
Rancho Mirage, California, United States
UCSD
San Diego, California, United States
Start Date
January 10, 2020
Primary Completion Date
April 1, 2028
Completion Date
April 1, 2028
Last Updated
March 3, 2025
NCT05647213
NCT06791850
NCT07399587
NCT06859970
NCT03180320
NCT05885607
Lead Sponsor
Endotronix, Inc.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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