Single Center Observational Study to Evaluate the Clinical Outcome of Patients with Bioabsorbable Vascular Scaffold (BVS, ABSORB® Abbot Vascular) after standard PCI Procedure.
- Conditions
- I20-I25Ischaemic heart diseases
- Registration Number
- DRKS00019947
- Lead Sponsor
- Hegau-Bodensee Kliniken Singen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Enrolling by invitation
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
(1) Patient received a BVS at the Hegau-Bodensee Clinic between 2013 and 2017, (2) Signed informed consent and privacy policy
Exclusion Criteria
(1) Patient age < 18 years, (2) Patient is not able to write and understand German
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method combined endpoint of Cardiac Death (CD), Myocardial Infarction (MI), Target Lesion Revascularization (TLR), Target Vessel Revascularization (TVR), Stent Thrombosis (ST)
- Secondary Outcome Measures
Name Time Method Quality of life measured by EQ-5D-5