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Ascorbic acid in contrast-induced nephropathy

Phase 3
Recruiting
Conditions
Acute coronary syndrome.
Acute coronary thrombosis not resulting in myocardial infarction
Registration Number
IRCT20151109024975N7
Lead Sponsor
Mazandaran University of Medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

patients undergoing angiography and contrast media
Contrast nephropathy score above 5
Age between 18-85

Exclusion Criteria

End stage Renal disease patients
Contrast usage 1 week before and 72 hours after study
Coadministration of nephrotoxic drug
Vitamin C usage during last 1 week

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ephropathy. Timepoint: 5 days. Method of measurement: creatine.
Secondary Outcome Measures
NameTimeMethod
????????. Timepoint: 1 week. Method of measurement: creatine.;Dialysis. Timepoint: 10 days. Method of measurement: Creatinin.;Mortality. Timepoint: 2 weeks. Method of measurement: patients follow up.
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