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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06348446
Other study ID # FY20-2963
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2022
Est. completion date August 30, 2024

Study information

Verified date March 2024
Source Seoul National University Hospital
Contact Sangil Min
Phone 01071739341
Email surgeonmsi@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Using CDW data from 5 tertiary hospitals in Korea, this study identify the optimal range of trough level that can prevent adverse outcome in the early periods after transplantation.


Recruitment information / eligibility

Status Recruiting
Enrollment 12000
Est. completion date August 30, 2024
Est. primary completion date July 30, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Renal transplant recipients between January 1, 2005 through December 31, 2014 in one of the five participating centers - Patients receiving oral tacrolimus as one of the main immunosuppressant at the start of the defined cohort time (i.e. at post-transplant 2 months for the analysis of 1-year outcomes and at post-transplant 12 months for the analysis of 6-year outcomes) Exclusion Criteria: - Graft failure occurring within the first 2 month of transplantation - Mortality of any cause occurring within the first 2 month of transplantation - Patients moving centers during the study period - Patients who have received other organ transplantation(s) besides renal transplantation in the defined period

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Asan medical center, Seoul, Korea Seoul
Korea, Republic of Samsung medical center, Seoul, Korea Seoul
Korea, Republic of Seoul St. Mary's hospital, Seoul, Korea Seoul
Korea, Republic of Severance hospital, Seoul, Korea Seoul

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital Astellas Pharma Inc

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary relationship between time varying periodic mean of tacrolimus trough and a composite 1-year allograft outcomes the relationship between time varying periodic mean of tacrolimus trough level during 2-12 mo. post-transplant and a composite of 1-year allograft outcomes consisting of biopsy proven acute rejection, renal dysfunction (eGFR<30), development of dnDSA, and death censored graft failure that occurred within 1 year from the latest transplant. 1 year after transplantation
Secondary relationship between time varying periodic mean of tacrolimus trough level during 12-72 mo. post-transplant and 6-year composite allograft outcome the relationship between time varying periodic mean of tacrolimus trough level during 12-72 mo. post-transplant and 6-year composite allograft outcome that occurred within 6 years from the latest transplant 6 year after transplantation
Secondary relationship between post-transplant time varying periodic mean tacrolimus trough level and severe infection the relationship between post-transplant time varying periodic mean tacrolimus trough level and severe infection (1-year and 6-year) 6 year after transplantation
Secondary relationship between post-transplant time varying periodic mean tacrolimus trough level and cardiovascular event the relationship between post-transplant time varying periodic mean tacrolimus trough level and cardiovascular event (1-year and 6-year) 6 year after transplantation
Secondary relationship between post-transplant time varying periodic mean tacrolimus trough level and patient mortality the relationship between post-transplant time varying periodic mean tacrolimus trough level and patient mortality (1-year and 6-year) 6 year after transplantation
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