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By invitation only Not applicable NCT07422688

Optical Coherence Tomography in Acute Vessel Evaluation

No applicable phase (e.g. observational)
Conditions: Ischemic Heart Disease Ischemic Coronary Artery Disease ACS (Acute Coronary Syndrome)

Sponsor: Aarhus University Hospital Skejby

trial.available_in: БГ
Overview
The purpose is to investigate if a strategy of routine OCT based diagnosis and guidance of PCI improves clinical outcomes compared with a standard strategy of guidance by angiography in patients presenting with ACS
Description
Patients presenting with acute coronary syndrome (ACS) have worse short and mid-term prognosis compared with patients revascularized for chronic coronary syndrome. Angiographic assessment of patients with ACS is frequently limited by high ambiguity both in identification of culprit lesions, characterization of non-culprit lesions, and in identification of suboptimal treatment results. Intravascular imaging may improve diagnosis and allow for better treatment optimization during coronary intervention of patients with ACS. The large-scale Chinese IVUS-ACS trial showed a 50% reduction in one-year MACE with IVUS-guided PCI in patients with ACS whereas a number of small studies on routine OCT guiding as well as ACS subgroups in RCTs did not indicate a potential similar benefit with OCT. OCT assessment has several theoretical advantages over IVUS in patients with ACS indicating the need for a well-designed strategy trial on OCT vs angiographic guided PCI. Hypothesis: Routine OCT-guided diagnosis and revascularization yields superior one-year clinical outcome compared with standard angiography-guided diagnosis and revascularization in patients with acute coronary syndrome Methods: Investigator initiated, open label, prospective, 1:1 randomized, multi-center, clinical outcome, superiority trial. Primary Endpoint: Major adverse cardiac events (MACE) comprising all-cause death, spontaneous myocardial infarction and stroke.
Who can participate
Inclusion Criteria: Clinical inclusion criteria: * NSTEMI, STEMI * Symptom duration \<12h for STEMI and \<48h for NSTEMI * Age ≥ 18yrs * Ability to provide written informed consent Angiographic inclusion criteria: * Angiographic signs of at least one possible culprit lesion. Signs including acute occlusion, partial occlusion, proximal embolus, haziness, high grade stenosis, stent thrombosis * Wire in true distal lumen Exclusion Criteria: Clinical exclusion criteria * Intravascular imaging evaluation of any lesions at index procedure * Cardiogenic shock * Sustained ventricular tachycardia or ventricular fibrillation * Planned CABG * Life expectancy \<1 year * Known severe heart failure with NYHA class equal or above III * Known ejection fraction \<30% before the admission * Known renal failure with GFR \<30 ml/min/1.73 m2 * Active bleeding or coagulopathy * Relevant allergies (contrast media, aspirin, clopidogrel, ticagrelor, everolimus) * Suspected inability to lie flat for the duration of the PCI procedure * Inability to comply with the planned follow-up program * Known or anticipated compliance problems with medical therapy Angiographic exclusion criteria * Study lesion involving the Left main coronary artery * Study lesion involving a true bifurcation lesion with a SB \>2.5mm * Severe tortuosity * Distal embolus * Isolated coronary artery spasm * Suspected spontaneous coronary artery dissection * Chronic total occlusions with treatment indication and no antegrade intra plaque wire pass
Interventions
Angiographic Guided PCI
PROCEDURE
OCT Guided PCI
PROCEDURE
Locations 18
Belgium (1)
Leuven University Hospital
Leuven
Denmark (5)
Aalborg University Hospital
Aalborg
Aarhus University Hospital Skejby
Aarhus N
Rigshospitalet
København Ø
Odense University Hospital
Odense
Zealand University Hospital, Roskilde Sygehus
Roskilde
Estonia (1)
North-Estonia Medical Centre
Tallinn
Finland (1)
North Karelia Central Hospital
Joensuu
Germany (2)
Vivantes Klinikum im Friedrichshain
Berlin
Universitätsklinikum Schleswig-Holstein Campus Kiel
Kiel
Italy (1)
Turin Nord Emergency Hospital
Turin
Latvia (1)
Latvia Centre of Cardiology
Riga
Netherlands (1)
Radboud University Medicine Center
Nijmegen
Norway (2)
Hospital of Southern Norway, Arendal
Arendal
Akerhus University Hospital - AHUS
Lørenskog
Sweden (1)
Sahlgrenska University Hospital
Gothenburg
Switzerland (1)
University Hospital of Zürich
Zurich
United Kingdom (1)
Royal Bournemouth Hospital
Bournemouth
Technical details
Status
By invitation only
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
23.11.2025
Completion date
01.09.2039
Registry ID
NCT07422688
Source
clinicaltrials.gov
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