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Effect of Nicorandil on contrast media-induced acute kidney injury

Phase 3
Conditions
Acute renal failure.
Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions
Registration Number
IRCT2016033118389N4
Lead Sponsor
Qom University of Medical Sciences and Health Services Vice chancellor
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
128
Inclusion Criteria

The inclusion criteria were the existence of at least one risk factor of contrast-induced nephropathy, including 1) Moderate systolic heart failure [30% < (EF) Ejection fraction < 45%] 2) Diabetes 3) Age> 75 years 4) Moderate renal insufficiency (1/5mg/ dL< Cr < 2mg/ dL 5) Hypotension (systolic blood pressure < 90 mm Hg 6) Anemia 7) History of hypertension Exclusion criteria: 1- Pregnancy and lactation 2- Allergy to radiographic contrast 3- Have cardiogenic shock and pulmonary edema during study 4- emergency catheterization 5- Serum creatinine levels> 2 mg/dL and preexisting dialysis 6- Exposure to contrast medium 48 h pre- and post-coronary angiography 7- Receive of diuretics, N-acetylcystein, sodium bicarbonate, Theophylline, Dopamine, Fenoldopam and NSAID’S during the study 8- Needs to continuous hydration therapy (e.g., sepsis) 9-severe heart failure (EF<=30%)

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum creatinine. Timepoint: Before and 48 h after contrast intake. Method of measurement: laboratory Kit (enzymatic method).
Secondary Outcome Measures
NameTimeMethod
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