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NCT04338503

Mechanically Optimizing Cardiac Preload in Heart Failure Patients

Status unknown Last updated 30 March 2023
What this trial tests

trial testing Partial IVC occlusion in Heart Failure in 10 participants. Status unknown.

Timeline
1 September 2021
Primary endpoint
30 June 2024
30 June 2024

Quick facts

Lead sponsorCardioflow Technologies, LLC
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment10
Start date1 September 2021
Primary completion30 June 2024
Estimated completion30 June 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Cardioflow Technologies, LLC

Who can join

Adults 18 to 80, any sex, with Heart Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the current study is to determine if partial balloon occlusion of the inferior vena cava can optimize cardiac pre-load and subsequently pulmonary pressures and cardiac output as a novel method to unload pulmonary edema and other symptoms of decompensated congestive heart failure. All products in this study are FDA approved and adhere to the specifications of the intended use.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Heart Failure

Currently open trials in the same condition.

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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/NCT04338503.

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