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NCT05015764

Reprieve Cardiovascular System for the Treatment of Subjects With Acute Decompensated Heart Failure Mechanistic Study

Completed NA Last updated 4 April 2025
What this trial tests

NA trial testing Fluid Management in Heart Failure in 31 participants. Completed in 2 May 2022.

Timeline
12 April 2021
Primary endpoint
2 May 2022
2 May 2022

Quick facts

Lead sponsorReprieve Cardiovascular, Inc
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposedevice feasibility
Enrollment31
Start date12 April 2021
Primary completion2 May 2022
Estimated completion2 May 2022
Sites1 location across Georgia

Drugs / interventions tested

Conditions studied

Sponsor

Reprieve Cardiovascular, Inc — full company profile →

Who can join

18 and older, any sex, with Heart Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Reprieve Cardiovascular System for the Treatment of Subjects with Acute Decompensated Heart Failure Mechanistic Study

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Edema formation in congestive heart failure and the underlying mechanisms.
    Abassi Z, Khoury EE, Karram T, Aronson D. · · 2022 · cited 48× · PMID 36237903 · DOI 10.3389/fcvm.2022.933215
  2. Novel Therapeutic Devices in Heart Failure.
    Guzik M, Urban S, Iwanek G, Biegus J, et al · · 2022 · cited 5× · PMID 35893394 · DOI 10.3390/jcm11154303

Verify or expand the search:

Other trials of Fluid Management

Trials testing the same drug.

Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Reprieve Cardiovascular, Inc trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05015764.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing