sefulness of 2mm coronary stent in percutaneous coronary intervention for Japanese patients with ischemic heart disease
Not Applicable
- Conditions
- Ischemic heart disease
- Registration Number
- JPRN-UMIN000038563
- Lead Sponsor
- Makiminato Central Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Not provided
Exclusion Criteria
1) Recurrent fatal ventricular arrhythmia 2) Anticoagulation therapy was required 3) Acute myocardial infarction within 72 hours 4) Planned PCI of any vessel within 30 days 5) Planned PCI of the target vessel(s) within 12 months 6) Blood disorder (such as hemophilia) 7) Bleeding tendency 8) Unsuitable for safe participation
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method