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OpenTrials
Completed

NCT Number: NCT04144660

"Treatment Use of ECMO In Pregnancy or Peripartum Patient."

The goal of this study is to describe the use of ECMO (Extracorporeal Membrane Oxygenation) in the pregnant or peripartum patient.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Female
  • Age 18 years or greater at the time of ECMO treatment.
  • Pregnant or within 6 months post-partum at the time of ECMO cannulation

Exclusion criteria

  • No history of pregnancy.
  • No treatment with ECMO.

Treatment and study plan

Extracorporeal membrane oxygenation

Device

Use of ECMO for circulatory / hemodynamic support of peripartum of pregnant patients who developed cardiogenic shock.

Primary outcomes

  1. Clinical Outcome of Mother

    Time frame: Time of diagnosis -Six Month Survival Rate

    Describe clinical course of pregnant or recently postpartum patients with cardiogenic shock treated with ECMO, including the rate of neonate survival

Sponsors and collaborators

Lead sponsor

Sarah Thordsen

Other

Collaborators

  • Medical College of Wisconsin

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Oct 30, 2019
Registry last updated
Nov 23, 2020

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.

Published trials that share one or more normalized conditions with this study.