Clinical effect of early loading of eicosepentaenoic acid after percutaneous coronary intervention in patients with acute coronary syndrome: a prospective, open-labeled, randomized controlled clinical trial
Not Applicable
- Conditions
- Acute coronary syndrome
- Registration Number
- JPRN-UMIN000016723
- Lead Sponsor
- Kagawa Prefectural Central Hopital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
cardiogenic shock, severe renal insufficiency requiring dialysis or continuous hemofiltration, cardiopulumonary arrest, emergency coronary artery bypass and failure of percutaneous coronary intervention.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method