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Study of factors (including genetic factors) influencing the levels of tacrolimus in blood before and after intake in renal transplant patients

Not Applicable
Conditions
Health Condition 1: null- Renal transplant patients on tacrolimus
Registration Number
CTRI/2013/08/003871
Lead Sponsor
Jawaharlal Institute of Post Graduate Medical Education and Research JIPMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

Subjects Age 18 to 65 years and of either gender.

Post renal transplant patients on treatment with tacrolimus

Exclusion Criteria

Subjects on parenteral immunosuppressants

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
pharmacokinetics parameters such as volume of distribution, clearanceTimepoint: predose, 0-2hrs, 2-4hrs, 4-12 hrs post dose
Secondary Outcome Measures
NameTimeMethod
pharmacokinetics parameters such as volume of distribution, clearanceTimepoint: single day
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