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Clinical Trial Details

Trial ID: L0882
Source ID: NCT01820195
Associated Drug: Oral N-Acetyl Cystein
Title: N-Acetyl Cystein and Contrast Nephropathy
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Chronic Kidney Disease Stage 2|Radiographic Contrast Agent Nephropathy
Interventions: DRUG: Oral N-Acetyl Cystein|DRUG: IV N-Acetyl Cystein|DRUG: Placebo group
Outcome Measures: Primary: Increase in serum creatinine more than 25% of baseline, 24 hours, 48 hours after exposure to contrast media | Secondary: Increase in serum creatinine more than 25% of baseline, The 5th day after exposure to contrast media
Sponsor/Collaborators: Sponsor: Imam Khomeini Hospital | Collaborators: Tehran Heart Center
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 549
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (CARE_PROVIDER, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
Start Date: 2013-03
Completion Date: 2014-11
Results First Posted:
Last Update Posted: 2013-03-28
Locations: Tehran Heart Center, Tehran, Iran, Islamic Republic of
URL: https://clinicaltrials.gov/show/NCT01820195