NCT04158479

Brief Summary

Extracorporeal life support (ECLS), also known as extracorporeal membrane oxygenation (ECMO), is an extracorporeal technique of providing effective cardiac and respiratory support to patients with lungs and/or heart failure. There was a growth in ECLS cases, centers, and center scale in China during the past decade. This multi-center registry was conducted by Chinese Society of Extracorporeal Life Support. The objectives were to investigate China statistics of ECLS and to evaluate the short-term and long-term outcomes of patients with ECLS.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20,000

participants targeted

Target at P75+ for all trials

Timeline
56mo left

Started Jan 2017

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress67%
Jan 2017Dec 2030

Study Start

First participant enrolled

January 1, 2017

Completed
2.8 years until next milestone

First Submitted

Initial submission to the registry

November 7, 2019

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 8, 2019

Completed
11.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2030

Last Updated

April 9, 2024

Status Verified

April 1, 2024

Enrollment Period

14 years

First QC Date

November 7, 2019

Last Update Submit

April 7, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • All-cause mortality

    30 days

Secondary Outcomes (5)

  • All-cause mortality

    365 days

  • Rate of successful weaning from ECMO

    30 days

  • ECMO-related complications

    30 days

  • Other complications

    30 days

  • Duration stay at ICU and hospital

    365 days

Study Arms (3)

Pulmonary Support

ECMO support for acute respiratory failure, ARDS

Device: ECMO

Cardiac Support

ECMO support for heart failure, cardiogenic shock

Device: ECMO

Extracorporeal Cardiopulmonary Resuscitation

ECMO support for cardia arrest

Device: ECMO

Interventions

ECMODEVICE

ECMO for circulatory and/or respiratory support

Cardiac SupportExtracorporeal Cardiopulmonary ResuscitationPulmonary Support

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients receiving ECMO for circulatory and/or respiratory support

You may qualify if:

  • Patients receiving ECMO for circulatory and/or respiratory support

You may not qualify if:

  • Refusal of consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Beijing, Beijing Municipality, 100029, China

RECRUITING

Related Publications (1)

  • Yuan Z, Liu Y, Wei G, Wang F, Yao B, Hou X, Xing J. Clinical characteristics of extracorporeal cardiopulmonary resuscitation in China: a multicenter retrospective study. BMC Anesthesiol. 2024 Jul 10;24(1):230. doi: 10.1186/s12871-024-02618-2.

MeSH Terms

Conditions

Shock, CardiogenicHeart ArrestHeart FailureRespiratory Distress Syndrome

Condition Hierarchy (Ancestors)

Myocardial InfarctionMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisShockLung DiseasesRespiratory Tract DiseasesRespiration Disorders

Central Study Contacts

Xiaotong Hou, MD., PhD.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief, Center for Cardiac Intensive Care

Study Record Dates

First Submitted

November 7, 2019

First Posted

November 8, 2019

Study Start

January 1, 2017

Primary Completion (Estimated)

December 31, 2030

Study Completion (Estimated)

December 31, 2030

Last Updated

April 9, 2024

Record last verified: 2024-04

Locations