OPtimal stEnt Deployment stRategy oF Contemporary sTents - Registry to Evaluate Percutaneous Coronary Intervention Using Bioresorbable Scaffolds With Thinner-strut Construction and Guidance by intracOronary Imaging to REduce Scaffold Failure

Inclusion Criteria: 1. Stable coronary artery disease with one or more significant epicardial stenosis in native coronary arteries suitable for OCT or IVUS-guided PCI with BRS implantation. 2. Subject must be at least 18 years of age 3. Written consent to participate in the study Exclusion Criteria: 1. Culprit lesions in the setting of acute coronary syndrome. 2. Lesions with severe calcification. 3. Lesions in a coronary artery with severe tortuosity. 4. Left main coronary artery lesions. 5. Bifurcation lesions. 6. Ostial lesions. 7. Lesions with a difference in proximal and distal reference diameter of \>0.5 mm by visual judgement of the coronary angiogram by the treating operator. 8. Treatment of in-stent restenosis or stent thrombosis. 9. History of definite stent thrombosis. 10. Lesions in coronary artery bypass grafts. 11. Lesions not suitable for OCT or IVUS catheter delivery and imaging, e.g. due to tortuosity or distal localisation. 12. Creatinine Clearance ≤ 30 ml/min/1.73 m2 as calculated by MDRD formula for estimated GFR. 13. Contraindication to dual antiplatelet therapy with aspirin and a P2Y12 inhibitor or (if indicated) NOAC and P2Y12 inhibitor. 14. Planned non-deferrable major surgery after PCI. 15. Known comorbidity associated with a life expectancy \<1 year. 16. Unable to understand and follow study-related instructions or unable to comply with study protocol.