Echocardiographic Assessment of Function During ECMO Support

Sponsor
Nationwide Children's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01551849
Collaborator
American Heart Association (Other)
5
1
60
0.1

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate echocardiographic markers of cardiac function to assess the ability of patients to successfully end VA-ECMO support.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    1. What is the major problem being addressed by this study?

    Extracorporeal membrane oxygenation (ECMO) is a machine used to do the work of the heart and lungs when children's hearts or lungs are too sick to perform normally. Veno-arterial (VA) ECMO therapy for poor heart function provides support that can lead to patient recovery, transplantation if appropriate and eligible, or complications of ECMO therapy lead to stopping care. Each day a patient is on ECMO, complications can occur that require stopping support, and attempting to get off ECMO as quickly as possible is important. There is currently no consistent way of assessing heart function while patients are supported by VA-ECMO to help guide when children's hearts have improved enough to survive without the help of ECMO.

    1. What specific questions are you asking and how will you attempt to answer them?

    The specific question we are asking is whether newer ultrasound measures of heart function can predict which patient may be well enough to be able to come off of ECMO support. We are following critically ill patients and performing multiple measurements at specific time points to look for changes in those patients whose heart function recovers and in those patients who do not recover function. The ultrasound measurements will be performed during changes in the amount of support provided by the ECMO machine.

      1. What is the long-term biomedical significance of your work, particularly as it pertains to the cardiovascular area? What major therapeutic advance(s) do you anticipate that it will lead to? For instance, new drug(s), a surgical technique/procedure, a diagnostic tool/test, a previously undetected risk factor, etc.

    Our long term goal is to develop non-invasive, quantitative measures of cardiac function for patients needing ECMO support to help guide care. Ultimately if deemed successful, these measurements could be used by all physicians who care for these patients. This study could lead to more efficient prediction of who needs to stay on ECMO and who could be removed. This could help to improve survival and decrease complications in some of the sickest children. These measurements may also help us to identify, at an early stage, those patients whose hearts are too sick to recover and will need a heart transplant evaluation.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    5 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Echocardiographic Assessment of Function During ECMO Support
    Actual Study Start Date :
    Jan 1, 2012
    Actual Primary Completion Date :
    Dec 30, 2016
    Actual Study Completion Date :
    Dec 30, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    VA-ECMO patients

    Patients placed on VA-ECMO support for primary cardiac dysfunction.

    Outcome Measures

    Primary Outcome Measures

    1. Ability to separate from VA-ECMO support with stable hemodynamics [48 hours]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • VA ECMO (all cannulation sites)

    • Primary Cardiac Failure

    • Septic Shock

    Exclusion Criteria:
    • VV ECMO

    • Primary Respiratory Failure

    • Congenital Diaphragmatic Hernia

    • Persistent pulmonary hypertension of the newborn

    • greater than 1 source of systemic perfusion

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nationwide Children's Hospital Columbus Ohio United States 43205

    Sponsors and Collaborators

    • Nationwide Children's Hospital
    • American Heart Association

    Investigators

    • Principal Investigator: Andrew R Yates, MD, Nationwide Children's Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nationwide Children's Hospital
    ClinicalTrials.gov Identifier:
    NCT01551849
    Other Study ID Numbers:
    • IRB11-00470
    • 12CRP9020022
    First Posted:
    Mar 13, 2012
    Last Update Posted:
    Jul 21, 2017
    Last Verified:
    Jul 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 21, 2017