ECPR-China: Registry Study of Extracorporeal Cardiopulmonary Resuscitation (eCPR) in China

• Sponsor: Peking Union Medical College Hospital (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT04956497
• Collaborator: (none)
• Enrollment: 300
• Location: 1
• Anticipated Duration (Months): 28
• Patients Per Site Per Month: 10.7

Study Details

Study Description

Brief Summary

The data of patients undergo extracorporeal cardiopulmonary resuscitation (eCPR) will be collected and analyzed. This study will provide useful information about the indication, the start time and others to improve the outcome of ECPR.

Condition or Disease	Intervention/Treatment	Phase
Extracorporeal Membrane Oxygenation Complication; Cardiopulmonary Arrest	Device: extracorporeal membrane oxygenation (ECMO)

Study Design

• Study Type: Observational [Patient Registry]
• Anticipated Enrollment: 300 participants
• Observational Model: Case-Only
• Time Perspective: Prospective
• Official Title: Registry Study of Extracorporeal Cardiopulmonary Resuscitation (eCPR) in China
• Anticipated Study Start Date: Sep 1, 2021
• Anticipated Primary Completion Date: Oct 31, 2023
• Anticipated Study Completion Date: Dec 31, 2023

Outcome Measures

Primary Outcome Measures

1. mortality rate [28 days]

   the death rate of the patients

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Age >=18y

• Cardiac arrested patients accept ECPR treatment

Exclusion Criteria:

• No

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Peking Union Medical College Hospital	Beijing		China	100730

Sponsors and Collaborators

• Peking Union Medical College Hospital

Investigators

• Study Chair: Jun Xu, MD, Peking Union Medical College Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Peking Union Medical College Hospital
• ClinicalTrials.gov Identifier: NCT04956497
• Other Study ID Numbers: PUMCH-001
• First Posted: Jul 9, 2021
• Last Update Posted: Jul 9, 2021
• Last Verified: May 1, 2021

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Heart Arrest

Study Results

No Results Posted as of Jul 9, 2021