RenalGuard System to Prevent Contrast-Induced Acute Kidney Injury in Japa
Not Applicable
- Conditions
- Chronic kidney disease with coronary aretry disease or peripheral artery disease
- Registration Number
- JPRN-UMIN000007308
- Lead Sponsor
- Yokohama Sakae Kyosai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
Class 3 or 4 chronic heart failure. Subject is anuric or has undergone renal replacement therapy, or has a known inability to have a Foley catheter placed. Subject has received contrast within 7 days of procedure. Subject has a known hypersensitivity to furosemide and/or the contrast agent being used.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method