Clinical Outcome of Liver Transplant Patients With Tacrolimus-based Immunosuppression
NCT ID: NCT03800576
Last Updated: 2021-03-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
113 participants
OBSERVATIONAL
2019-06-06
2020-09-22
Brief Summary
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Detailed Description
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This is a retrospective study. Eligible patients were those who had signed informed consent for genetic study in previous research projects ( IRB approval number:201512005RINC and 201612023RIND ). The present study will collect laboratory data, concurrent medications, and therapeutic drug monitoring (TDM) data. Patient survival, graft survival, acute rejection and tacrolimus-associated adverse events will be assessed.
Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* at the age of 20-65
* with tacrolimus-based immunosuppression after liver transplant for at least 6 months.
Exclusion Criteria
* multi-organ transplantation
* human immunodeficiency virus (HIV) positive.
20 Years
65 Years
ALL
No
Sponsors
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National Taiwan University Hospital
OTHER
Responsible Party
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Principal Investigators
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Rey-Heng Hu, Professor
Role: PRINCIPAL_INVESTIGATOR
National Taiwan University Hospital
Locations
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National Taiwan University Hospital
Taipei, , Taiwan
Countries
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Other Identifiers
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201812015RINC
Identifier Type: -
Identifier Source: org_study_id
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