Chronic Total Coronary Occlusion Treatment Results 6 Years After Bioresorbable Scaffold Implantation
CompletedNot applicableNCT06164977
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Aim of the study is to evaluate chronic total coronary occlusion treatment results 6 years after bioresorbable scaffold implantation by quantitative coronary analysis, intravascular ultrasound and optical coherence tomography.
Study details
- Official title
- Chronic Total Coronary Occlusion Treatment Results 6 Years After Bioresorbable Scaffold Implantation
- Conditions
- Angina Pectoris
- Coronary Artery Disease
- Occlusion, Coronary
- Interventions
- Procedure: Percutaneous coronary intervention.
- Sponsor
- Pauls Stradins Clinical University Hospital
- Start date
- 2017-02-01
- Primary completion
- 2023-12-01
- Sex
- All
- Results posted
- No results posted in this snapshot
- Countries
- Latvia
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 100% occlusion of a coronary artery for a duration of greater than or equal to 3 months based on angiographic evidence. Exclusion Criteria: * Participant withdrawal from study.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06164977