RecruitingNot ApplicableNCT03392415
The NOrdic-Baltic Randomized Registry Study for Evaluation of PCI in Chronic Total Coronary Occlusion
The NOrdic-Baltic Randomized Registry Study for Long-term Clinical Evaluation of Adjunction of PCI to Optimal Medical Therapy in Chronic Total Coronary Occlusion
Sponsor
Leif Thuesen
Enrollment
2,000 participants
Start Date
Jun 1, 2018
Study Type
INTERVENTIONAL
Conditions
Summary
Randomized registry for the study of CTO PCI as adjunction to optimal medical therapy.
Eligibility
Min Age: 18 Years
Inclusion Criteria4
- ≥1 CTO lesion amenable to PCI.
- Stable and stabilized coronary artery disease
- Symptoms (angina pectoris or shortness of breath) and/or signs of reversible perfusion defect by SPECT, PET or MR and/or angiographic/echocardiographic indication of reversible ischemia.
- CTO lesion in a major coronary vessel supplying a significant myocardial territory (vessel diameter usually ≥3mm).
Exclusion Criteria5
- Expected survival \<1 year.
- Renal failure on dialysis.
- Stable non-CTO lesions treated within one month.
- Declined informed consent.
- Regarding CMR: allergy to contrast medium, severe obesity, claustrophobia and certain metallic implants
Interventions
PROCEDURECTO PCI
attempted percutaneous coronary intervention of the chronic total coronary occlusion
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03392415
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