Trial ID: | L0295 |
Source ID: | NCT01210456
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Associated Drug: |
Physiological Saline, N-Acetylcysteine And Sodium Bicarbonate
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Title: |
Efficacy Trial of N-Acetylcysteine and Sodium Bicarbonate for the Prevention of Contrast-Induced Acute Kidney Injury
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Acronym: |
PREKIT
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Status: |
UNKNOWN
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Study Results: |
NO
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Results: |
|
Conditions: |
Chronic Kidney Disease
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Interventions: |
DRUG: Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
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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
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Sponsor/Collaborators: |
Sponsor: Tokushukai Medical Group
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE3
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Enrollment: |
458
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: PREVENTION
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Start Date: |
2009-10
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Completion Date: |
2014-11
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Results First Posted: |
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Last Update Posted: |
2014-09-16
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Locations: |
Sapporo Higashi Tokushukai Hospital, Sapporo City, Hokkaido, 065-0033, Japan
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URL: |
https://clinicaltrials.gov/show/NCT01210456
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