Comparison of 2 contrast agents in preventing acute renal failure after angiography
Phase 1
- Conditions
- Peripheral vascular or renovascular disease being investigated by angiography
- Registration Number
- EUCTR2005-001986-32-GB
- Lead Sponsor
- HS Tayside
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Patients over age of 18 undergoing routine angiography as part of the investigation of peripheral or renovascular disease
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Inability to consent
Children (below age 18)
Pregnancy and lactation
Women of child-bearing age (below 55 years)
Recent (less than 7 days) administration of any iodinated contrast agent similar to test products
Dialysis dependent renal failure
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method