- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04477967
Design and Implementation of the Pediatric Liver Transplantation Biobank
July 15, 2020 updated by: Qiu Li, Children's Hospital of Chongqing Medical University
Children's Hospital of Chongqing Medical University
The purpose of the pediatric liver transplant biobank is to systematically collect clinical specimens from pediatric end-stage liver disease.
It is expected to contribute to the research and development of paediatric end-stage liver disease in the future.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
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: Xiang Zheng
- Phone Number: 17723191712
- Email: xiangzheng061@163.com
Study Locations
-
-
Chongqing
-
Chongqing, Chongqing, China, 400014
- Recruiting
- Children's Hospital of Chongqing Medical University
-
-
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 month to 18 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Children with end-stage liver disease who undergo liver transplantation in our hospital.
Obtain their or their parents' informed consent before the project starts.
Description
Inclusion Criteria:
- Children diagnosed with end-stage liver disease.
- Liver transplantation in our hospital.
- informed patient consent.
- long-term follow-up in our hospital.
Exclusion Criteria:
No fixed contact information, difficult to follow up the patients.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Biological sample bank
Time Frame: 2 years
|
A repository of biological samples from patients who will join the project, will be organised at the biobank center of the Children's Hospital of Chongqing Medical University(CHCMU) under the responsibility of the experienced staff at the Department of Hepatic.
|
2 years
|
Integrated health data platform
Time Frame: 2 years
|
Collect patient clinical test information and establish diagnostic database.
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
October 1, 2018
Primary Completion (Anticipated)
January 1, 2021
Study Completion (Anticipated)
July 1, 2028
Study Registration Dates
First Submitted
July 8, 2020
First Submitted That Met QC Criteria
July 15, 2020
First Posted (Actual)
July 20, 2020
Study Record Updates
Last Update Posted (Actual)
July 20, 2020
Last Update Submitted That Met QC Criteria
July 15, 2020
Last Verified
July 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018(120)
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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