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acetylcysteine as a Preventive Measure for Contrast Induced Nephropathy in Intensive Care Patients with Renal Insufficiency

Completed
Conditions
Renal insufficiency
Urological and Genital Diseases
Registration Number
ISRCTN43635237
Lead Sponsor
Academic Medical Centre (AMC) (Netherlands)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
246
Inclusion Criteria

1. (Chronic or acute) renal insufficiency (not presently on renal replacement therapy) defined as a plasma creatinine greater than 180 µmol/L
2. Planned diagnostic imaging procedure requiring the use of intravenous radiographic contrast agents
3. Admitted to one of the participating intensive care units

Exclusion Criteria

1. Pregnancy
2. No informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Rise in plasma creatinine greater than 25% within 48 hours after contrast administration<br>2. Need for Continuous Venous-Venous Haemofiltration (CVVH) therapy at any moment during stay in ICU<br>3. Duration of CVVH therapy, if initiated<br>4. Renal insufficiency (for which ongoing renal replacement therapy) at ICU-discharge
Secondary Outcome Measures
NameTimeMethod
o secondary outcome measures
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