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Effect of vitamin E in preventing kidney problems in thalassemia patients

Phase 3
Conditions
N17.0
E72.0
R94.4
Condition 1: Thalassemia. Condition 2: Acute Kidney Injury. Condition 3: Fanconi syndrome. Condition 4: Abnormal Kidney function.
Beta thalassemia
Acute kidney failure with tubular necrosis
Disorders of amino-acid transport
Abnormal results of kidney function studies
D56.1
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
NameTimeMethod
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
NameTimeMethod
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