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NCT Number: NCT06336655

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 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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Utah

Salt Lake City, Utah, 84132, United States

Location status: Recruiting

Location contact

Joseph E. Tonna, MD, FAAEM

CONTACT

[email protected]

801.587.9373

About this study

Although extracorporeal membrane oxygenation (ECMO) for cardiogenic shock (CS) is used in over 3,000 patients per year, the best management strategies are not known. Identifying and improving treatment of CS is critically important, as CS occurs in 160,000 patients per year in the US with a 50% mortality rate. VA ECMO is an increasingly used method of mechanical circulatory support (MCS) for patients with CS refractory to medical therapy. Despite the benefit of full cardiopulmonary support ECMO is also thought to increase after load in the failing heart- which paradoxically reduces cardiac output and may lead to myocardial injury and cardiac congestion. A potential solution is to add a device to VA ECMO that decreases after-load - known as left ventricular (LV) unloading. LV unloading can be achieved with different approaches, directly with transvalvular pumps (known as a peripheral ventricular assist device (pVAD)), or indirectly with an intra-aortic balloon pump (IABP)

Preliminary data suggests that unloading the LV is associated with improved survival. Results from a cohort of VA ECMO patients with medical CS, showed a hospital survival benefit LV unloading (aOR 0.87 (0.79, 094); p=0.001). Data has also shown that the survival benefit of LV unloading was much larger with pVAD (HR 0.6), but with higher complications, including limb ischemia - a potentially catastrophic complication. However, results also show that different unloading approaches have different physiologic effects on the myocardium and on peripheral perfusion - highlighting the uncomfortable observation that it is not known how (physiologically) these unloading devices lead to changes in survival.

There are two potential pathways whereby LV unloading could influence survival, including myocardial effects (distension, injury, ejection fraction ) and peripheral effects (peripheral pulse pressure, lactate clearance, CO2 gap). Determining the physiologic effects from LV unloading according to device type and patient etiology will allow us to match the intervention with the patient's physiology. Data suggests that ECMO patients with acute myocardial infarction (AMI) have different mortality and different physiologic changes than patients with decompensated chronic heart failure (CHF) when unloaded.

The ultimate goal is to reduce morbidity and mortality in cardiogenic shock. This study will define the physiologic benefit of LV unloading during CS.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (age 18 years or older)
  • Diagnosis of acute cardiogenic shock (CS)
  • Patients failing medical therapy, defined as 1 or more of the following:
  • Society for Coronary Angiography and Interventions (SCAI) Stage C or greater
  • 2 or more inotropic medications and not improving
  • IABP in place and clinically worsening
  • Placed on VA ECMO for CS
  • In the opinion of the attending physician, patient has worsening CS and could require VA ECMO support in the near-term

Exclusion criteria

  • Metastatic or stage 4 cancer
  • Atrial septostomy
  • Planned LV unloading on ECMO
  • Anticipated death <72 hours
  • Existing durable left ventricular assist device (dLVAD)
  • Unwillingness to randomize
  • Patients who are pregnant

Treatment and study plan

IABP

Device

LV unloading via intra-aortic balloon pump (IABP)

Other names: LV unloading

Primary outcomes

  1. Change in pulmonary capillary wedge pressure

    Time frame: ECMO start, ECMO day 5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in pulmonary capillary wedge pressure (PCWP) from ECMO start to ECMO day 5 (Day 5 - Baseline) with and without LV unloading

Secondary outcomes

  1. Change in pulmonary artery diastolic pressure

    Time frame: ECMO start, ECMO days 1-5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in pulmonary artery diastolic pressure (PADP) from ECMO start to ECMO day 5 (Day 5 - baseline) with and without LV unloading

  2. Change in left ventricular end diastolic diameter

    Time frame: ECMO start, ECMO day 5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in left ventricular end diastolic diameter (LVEDd) from ECMO start to ECMO day 5 (Day 5 - baseline) with and without LV unloading

  3. Change in N-terminal pro b-type natriuretic peptide

    Time frame: ECMO start, ECMO days 1-5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in N-terminal pro b-type natriuretic peptide (NT-pro BNP) from ECMO start to ECMO day 5 (Day 5 - baseline) with and without LV unloading

  4. Hemodynamic stability

    Time frame: ECMO start, ECMO day 5

    Hemodynamic stability (defined as a change in mean arterial pressure [MAP] from prior to turn down until 2 minutes of wean) at ECMO day 5 with and without LV unloading

  5. Global cardiovascular function

    Time frame: ECMO start, ECMO days 1-5

    Global cardiovascular function is defined as arterial pulse pressure during the protocoled wean. To assess this outcome, the investigators will calculate the change in pulse pressure from prior to wean to 2 minutes during wean.

  6. Difference in partial pressure of carbon dioxide (pCO2)

    Time frame: ECMO start, q12 hours ECMO days 1-3, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    As part of assessing global cardiovascular function, the investigators will measure, via lab draw, pCO2, which is the difference in CO2 between arterial and central venous blood. This is a marker of peripheral perfusion.

  7. Lactate

    Time frame: ECMO start, ECMO days 1-5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    As part of assessing global cardiovascular function, the investigators will measure, via lab draw, arterial lactate. This is a marker of peripheral perfusion.

  8. Cardiac BIN1

    Time frame: ECMO start, ECMO day 5, day of ICU discharge up to 6 months

    Change in Cardiac BIN1 (cBIN1) serum level from Baseline to Day 5 (Day 5 - Baseline). cBIN1is a validated marker of myocardial recovery in heart failure.

  9. Troponin I

    Time frame: ECMO start, ECMO days 1-5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in troponin I from ECMO start to ECMO day 5 (Day 5 - Baseline)

  10. Tumor necrosis factor alpha

    Time frame: ECMO start, ECMO day 5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Change in tumor necrosis factor alpha (TNFa) from ECMO start to ECMO day 5 (Day 5 - Baseline)

  11. Ejection fraction percentage

    Time frame: ECMO start, ECMO day 5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Assessment of heart function via echocardiography

  12. Interferon gamma

    Time frame: ECMO start, ECMO day 5, ECMO decannulation up to 3 months, day of ICU discharge up to 6 months

    Predictor of myocardial recovery assessed from baseline through ICU discharge

  13. Limb ischemia

    Time frame: Randomization, 48 hours post-device removal

    Ischemia in the ipsilateral limb as the IABP will be tracked from baseline until 48 hours after the intervention is removed.

  14. Mortality

    Time frame: Hospital discharge up to 6 months

    Assessment of patient mortality status at hospital discharge

Sponsors and collaborators

Lead sponsor

University of Utah

Other

Collaborators

  • University of Minnesota

Registry information

Important dates

Study start
2024
Primary completion
2028
Study completion
2029
First posted
Mar 29, 2024
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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