Effect of vitamin E in preventing kidney problems in thalassemia patients
Phase 3
- Conditions
- N17.0E72.0R94.4Condition 1: Thalassemia. Condition 2: Acute Kidney Injury. Condition 3: Fanconi syndrome. Condition 4: Abnormal Kidney function.Beta thalassemiaAcute kidney failure with tubular necrosisDisorders of amino-acid transportAbnormal results of kidney function studiesD56.1
- Registration Number
- IRCT20221111056466N1
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
All patients with thalassemia are covered by Amir Kabir Arak Hospital
Exclusion Criteria
All patients who are covered by Amirkabir Hospital but do not consent to participate in the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Creatinine level. Timepoint: It will be checked on the first day of the study and 48 hours and 7 days after the start of the study. Method of measurement: blood samples.;Glomerular filtration rate. Timepoint: It will be checked on the first day of the study and 48 hours and 7 days after the start of the study. Method of measurement: blood sample.;Blood phosphorus level. Timepoint: It is checked on the first day of the study and 30 days after the start of the study. Method of measurement: blood sample.;Urine glucose level. Timepoint: It is checked on the first day of the study and 30 days after the start of the study. Method of measurement: urine sample.;Venous blood gas level. Timepoint: It is checked on the first day of the study and 30 days after the start of the study. Method of measurement: blood sample.;The ratio of blood urea nitrogen to creatinine. Timepoint: It is checked on the first day of the study and 30 days after the start of the study. Method of measurement: blood sample.
- Secondary Outcome Measures
Name Time Method