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NCT06336655 · ClinicalTrials.gov registry record · Phase 2

Physiology of Unloading VA ECMO Trial

A Phase 2 study of Cardiogenic Shock, sponsored by University of Utah.

Recruiting
Registry status
Phase 2
Development phase
104
Enrollment target
1
Study location

NCT06336655 is a Phase 2 study of Cardiogenic Shock that is actively recruiting participants, run by University of Utah. The registered enrollment target is 104 participants, below the 628-participant average among 16 other Cardiogenic Shock trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06336655, a Phase 2 study of Cardiogenic Shock, is actively recruiting participants, sponsored by University of Utah.

RECRUITING
Registry status
Phase 2
Development phase
104 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to compare the use of veno-arterial extracorporeal membrane oxygenation (VA ECMO) with and without left ventricular (LV) unloading in patients being treated for cardiogenic shock (CS). The main aims of the study are: 1. To determine the physiologic effects on cardiopulmonary congestion of adding LV unloading to VA ECMO 2. To determine the effects on myocardial function of adding LV unloading to ECMO 3. To test the effects on myocardial recovery of adding LV unloading to VA ECMO Participants who are being treated with VA ECMO will be randomized to receive or not receive LV unloading in the form of an intra-aortic balloon pump (IABP). Over the course of the study, the investigators will obtain measurements via lab work, echocardiography, and pulmonary artery catheter that will allow comparison of the two groups.

Conditions Studied

Interventions

  • DEVICE IABP

Study Locations (1)

Utah

  • University of Utah - Salt Lake City

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2024-10-02
Est. Completion 2029-02-01
Phase Phase 2

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT06336655

The ClinicalTrials.gov registry entry for NCT06336655 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 104 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 628-participant average among 16 other Cardiogenic Shock trials with a reported enrollment target (83% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cardiogenic Shock appearing as the primary indexed condition, and to 1 intervention - of which IABP is the first listed.

NCT06336655 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.

Frequently Asked Questions

What is clinical trial NCT06336655 about?

NCT06336655 is a clinical study titled "Physiology of Unloading VA ECMO Trial". The goal of this clinical trial is to compare the use of veno-arterial extracorporeal membrane oxygenation (VA ECMO) with and without left ventricular (LV) unloading in patients being treated for cardiogenic shock (CS). The main aims of the study are: 1. To determine the physiologic effects on card...

What is the current status of trial NCT06336655?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 104 participants. The study started on 2024-10-02. Estimated completion is 2029-02-01.

What conditions does trial NCT06336655 study?

This clinical trial studies the following conditions: Cardiogenic Shock.

What interventions are being tested in trial NCT06336655?

The interventions under investigation include: IABP (DEVICE).

Who is sponsoring clinical trial NCT06336655?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06336655 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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