Actively Recruiting

All Genders
ID04158479

China Extracorporeal Life Support Registry Observational Study on ECMO Use in Heart and Lung Failure

Led by Beijing Anzhen Hospital · Updated on 2024-04-09

20000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Extracorporeal life support (ECLS), also called extracorporeal membrane oxygenation (ECMO), is a technique that helps support the heart and lungs in patients with heart failure, lung failure, or both. In China, the use of ECLS has grown over the past decade, with more cases and more centers adopting this technology. This multi-center registry study, led by the Chinese Society of Extracorporeal Life Support, aims to collect data on the use of ECLS in China and evaluate both short-term and long-term patient outcomes. The study includes patients receiving ECMO for different conditions such as acute respiratory failure, acute respiratory distress syndrome (ARDS), heart failure, cardiogenic shock, and cardiac arrest. Data are collected from multiple hospitals across China to capture real-world use of ECMO as a device providing circulatory and respiratory support. Different groups in the registry represent pulmonary support, cardiac support, and extracorporeal cardiopulmonary resuscitation. Participants in the study have their health outcomes observed and recorded, including 30-day and 365-day all-cause mortality, rates of successful ECMO weaning, ECMO-related and other complications, and length of stay in intensive care units and hospitals. This observational study monitors these measures to better understand the effects and outcomes associated with ECMO treatment over time. The study began in 2017 and is planned to continue through 2030.

CONDITIONS

Brief Title

China Extracorporeal Life Support Registry

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients receiving ECMO for circulatory and/or respiratory support
Not Eligible

You will not qualify if you...

  • Refusal of consent to participate in the study

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Varies based on treatment duration

Participants receive ECMO support for circulatory and/or respiratory failure as part of routine care. Data on their ECMO treatment and outcomes are collected.

Long-term Monitoring

Duration - Up to 365 days

Participants are observed for short-term and long-term outcomes following ECMO treatment, including mortality and complications up to 365 days.

Trial Site Locations

Total: 1 location

1

Center for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University

Beijing, Beijing Municipality, China, 100029

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Research Team

X

Xiaotong Hou, MD., PhD.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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