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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: JPRN
Last refreshed on: 17 October 2023
Main ID:  JPRN-UMIN000008004
Date of registration: 21/05/2012
Prospective Registration: No
Primary sponsor: Tokyo Women's Medical University
Public title: Analysis of efficacy and safety of tacrolimus extended-release formulation on prevention of rejection and GVHD in allo-HSCT patients
Scientific title: Analysis of efficacy and safety of tacrolimus extended-release formulation on prevention of rejection and GVHD in allo-HSCT patients - Efficacy and safety of tacrolimus extended-ralease formulation
Date of first enrolment: 2012/05/01
Target sample size: 15
Recruitment status: Pending
URL:  https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009408
Study type:  Observational
Study design:  Not selected Not selected  
Phase:  Not selected
Countries of recruitment
Japan
Contacts
Name:    
Address:  Japan
Telephone:
Email:
Affiliation:  Tokyo Women's Medical University Department of Hematology
Name:     Toshiko Motoji
Address:  8-1 Kawada-cho, Shinjuku-ku, Tokyo Japan
Telephone:
Email:
Affiliation:  Tokyo Women's Medical University Department of Hematology
Key inclusion & exclusion criteria
Inclusion criteria:
Exclusion criteria: 1. patients who had allergic reaction to tacrolimus 2. patients with the administration ofcyclosporin A or bosentan 3. patients with the administration of potassium-conserving diuretic 4. patients who are pregnant or have the possiblity of pregnancy

Age minimum: 20years-old
Age maximum: Not applicable
Gender: Male and Female
Health Condition(s) or Problem(s) studied
allo hematopoietic stem cell transplantations of hematopoietic disorders
Intervention(s)
Primary Outcome(s)
Analysis of efficacy and safety of tacrolimus extended-release formulation on prevention of rejection and GVHD
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Tokyo Women's Medical University
Secondary Sponsor(s)
Ethics review
Status: YES
Approval date:
Contact:
Results
Results available:
Date Posted:
Date Completed:
URL:
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