Slender sheath/guiding catheter combination versus sheathless guiding catheter for acute coronary syndrome: A propensity-matched analysis of the two devices
Phase 4
- Conditions
- Acute coronary syndrome (ACS), including ST-elevation myocardial infarction and non-ST-elevation ACS
- Registration Number
- JPRN-UMIN000040498
- Lead Sponsor
- Sendai Kousei Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 1108
Inclusion Criteria
Not provided
Exclusion Criteria
The exclusion criteria were as follows: (i) PCI via femoral or brachial access, (ii) transradial PCI using guiding catheter systems other than 7.5-Fr sheathless Eaucath guiding catheters or 7-Fr Glidesheath slender sheaths/7-Fr Hyperion guiding catheter (Asahi Intecc) combination, (iii) refusal to participate, and (iv) loss of follow-up.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The endpoints were radial artery occlusion at 30 days, severe radial spasm during PCI, access-site major bleeding within 30 days as defined by the Bleeding Academic Research Consortium type 3 or 5 criteria, coronary ostial dissection by the guiding catheters, and procedural success.
- Secondary Outcome Measures
Name Time Method