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Evaluation of the effects of Calcitriol on acute kidney injury

Not Applicable
Conditions
acute kidney injury.
acute renal impairment
Registration Number
IRCT2016022326716N1
Lead Sponsor
Vice Chancellor for Research Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
122
Inclusion Criteria

age:18 years old or more; voluntary participation in the study?.admission in ordinary wards, CCU, ICU
Exclusion criteria:
Using vitamin D or its derivatives at the time of study initiation;the type of malignancies that lead to calcium level more than 10.5mg/dl;serum calcium level more than 10.5mg/dl

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maximum creatinin level. Timepoint: daily. Method of measurement: blood sampling.;Number of dialysis sessions during admission. Timepoint: daily. Method of measurement: researcher made checklist.;Admission duration. Timepoint: daily. Method of measurement: researcher made checklist.;Recovery duration. Timepoint: daily. Method of measurement: researcher made checklist.;Becoming CKD. Timepoint: monthly up to three months. Method of measurement: serum creatinin measurement.;Mortality rate. Timepoint: three months maximum. Method of measurement: researcher made checklist.
Secondary Outcome Measures
NameTimeMethod
Hyperphosphatemia. Timepoint: during three months. Method of measurement: blood sampling.;Hypercalcemia. Timepoint: during three months. Method of measurement: blood sampling.
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