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The effect of intravenous iron therapy and erythropoesis-stimulation agent combination on renal transplant outcomes

Not Applicable
Recruiting
Conditions
Diseases of the genitourinary system
Registration Number
KCT0008143
Lead Sponsor
Yonsei University Health System, Severance Hospital
Brief Summary

Not available

Detailed Description

Not available

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
NameTimeMethod
Comparison of the number of blood transfusions according to the combination of intravenous iron therapy and EPO agent on perioperative period
Secondary Outcome Measures
NameTimeMethod
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
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