Logo 1 Logo 2

Clinical Trial Details

Trial ID: L0295
Source ID: NCT01210456
Associated Drug: Physiological Saline, N-Acetylcysteine And Sodium Bicarbonate
Title: Efficacy Trial of N-Acetylcysteine and Sodium Bicarbonate for the Prevention of Contrast-Induced Acute Kidney Injury
Acronym: PREKIT
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Chronic Kidney Disease
Interventions: DRUG: Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
Outcome Measures: Primary: Development of contrast-induced acute kidney injury, Contrast-Induced Acute Kidney Injury(CIAKI) was defined as an absolute increase in serum creatinine of more than or equal to 0.3mg/dl (≥ 26.4 μmol/l), a percentage increase in serum creatinine of more than or equal to 50% (1.5-fold from baseline) within 48 hours of intravascular contrast administration in the absence of any alternative causes, or a reduction in urine output documented oliguria of less than 0.5 ml/kg per hour for more than six hours., within 48 hours | Secondary: Requirement of dialysis, 6 months|Requirement of hospitalization and death, 6 months
Sponsor/Collaborators: Sponsor: Tokushukai Medical Group
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 458
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: PREVENTION
Start Date: 2009-10
Completion Date: 2014-11
Results First Posted:
Last Update Posted: 2014-09-16
Locations: Sapporo Higashi Tokushukai Hospital, Sapporo City, Hokkaido, 065-0033, Japan
URL: https://clinicaltrials.gov/show/NCT01210456