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Mechanically Optimizing Cardiac Preload in Heart Failure Patients

NCT04338503 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2023-03-30

No results posted yet for this study

Summary

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.

Conditions

Interventions

DIAGNOSTIC_TEST

Partial IVC occlusion

Partial balloon occlusion of the inferior vena cava.

Sponsors & Collaborators

  • Saint Thomas Health

    collaborator OTHER

  • Cardioflow Technologies, LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2024-06-30
Completion
2024-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04338503 on ClinicalTrials.gov