- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04709432
ECMO Treatment of Children in China in the Past 10 Years
February 6, 2024 updated by: Children's Hospital of Fudan University
Extracorporeal Membrane Oxygenation (ECMO) Treatment of Children in Mainland China in the Past 10 Years
It is a cross-sectional study to summarize the extracorporeal membrane oxygenation (ECMO)treatment in children in China.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
ECMO treatment in children is still in its infancy in China, and it has made considerable progress in recent years.
In order to further understand the development of ECMO treatment in critically ill children, the investigator conduct this cross-sectional research through questionnaires.
The investigator collect general information of the hospital and ECMO equipment, etiology, compilation, and mode of ECMO.
Study Type
Observational
Enrollment (Estimated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: YING JIAYUN
- Phone Number: 18817583962
- Email: jiayundoctor@163.com
Study Locations
-
-
Shanghai
-
Shanghai, Shanghai, China
- Recruiting
- Children's Hospital of Fudan University
-
Contact:
- Guoping Lu, MD
- Phone Number: 18017590817
- Email: 13788904150@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 day to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
children supported by ECMO in mainland China in the past years
Description
Inclusion Criteria:
- age of 1d to 18 years old;
- children supported by ECMO in mainland China in the past 10 years
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
ECMO group
children supported by ECMO in the past 10 years
|
ECMO is a form of Extracorporeal Life Support (ECLS) to support either the pulmonary, or both the pulmonary and cardiac systems.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
survival rate
Time Frame: from admission to discharge (about 10days)
|
survival rate after discharge
|
from admission to discharge (about 10days)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
time of running ECMO
Time Frame: from admission to discharge(about 10days)
|
the total time of running ECMO
|
from admission to discharge(about 10days)
|
cost of ECMO treatment
Time Frame: from admission to discharge (about 10days)
|
the total cost of ECMO treatment
|
from admission to discharge (about 10days)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Lu Guoping, Children's Hospital of Fudan University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 11, 2021
Primary Completion (Estimated)
December 31, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
January 13, 2021
First Submitted That Met QC Criteria
January 13, 2021
First Posted (Actual)
January 14, 2021
Study Record Updates
Last Update Posted (Actual)
February 7, 2024
Last Update Submitted That Met QC Criteria
February 6, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- fdpicu-06
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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