The effect of intravenous iron therapy and erythropoesis-stimulation agent combination on renal transplant outcomes
Not Applicable
Recruiting
- Conditions
- Diseases of the genitourinary system
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 302
Inclusion Criteria
1. living donor transplantation (Age >19)
2. Ferririn<700?/L, TSAT<40%
Exclusion Criteria
1. subject who is CDC(+), FXM(+)
2. Subject with a active infection
3. Hematologic malignancy, monoclonal gammaglobulin Dz, Hematologic Dz induced anemia
4. Receiving treatment of malignant tumor
5. Subject who is HIV(+)
6. Recent(within 3 months) participation in an interventional trial
7. ALT, AST >3 times upper limit of normal
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of the number of blood transfusions according to the combination of intravenous iron therapy and EPO agent on perioperative period
- Secondary Outcome Measures
Name Time Method comparison of changes in anemia parameters(ferritin, TSAT, EPO level) following the administraiton of intravenous iron therapy and EPO agent;comparison of changes in hepcidin expression level following the administraiton of intravenous iron therapy and EPO agent;comparison of changes in oxidative stress marker following the administraiton of intravenous iron therapy and EPO agent;comparison of changes in immunologic parameters(de novo DSA, antibody-mediated rejection rate, death censored graft survivial and patient survival rate) following the administraiton of intravenous iron therapy and EPO agent