Testing early versus delayed heart angiography with medicine in chronic chest pain

Trial details

Who runs it

Gødstrup Hospital

Trial code

NCT05865600

Record updated

10 December 2025

Original description

We will establish a cohort of 570 symptomatic chronic coronary syndrome patients undergoing 15O-water PET and assess their symptoms through repeated questionnaires. Two hundred patients with abnormal perfusion will be randomized to immediate or delayed referral to invasive coronary angiography with concomitant optimization of guideline-directed medical therapy with repeated 15O-water PET and questionnaires at 3 and 6 months. The primary objective is to compare the potential benefit of early invasive coronary angiography (ICA) versus guideline directed medical therapy (GDMT) on symptomatic relief defined as freedom of angina after 3 months following a positive [15O]H2O cardiac PET/CT in patients with symptomatic chronic coronary syndrome.Read full original descriptionShow less

Perfusion Estimation for Optimal Revascularization and Medical Therapy in Chronic Coronary Syndrome - a Randomized Trial

We will establish a cohort of 570 symptomatic chronic coronary syndrome patients undergoing 15O-water PET and assess their symptoms through repeated questionnaires. Two hundred patients with abnormal perfusion will be randomized to immediate or delayed referral to invasive coronary angiography with concomitant optimization of guideline-directed medical therapy with repeated 15O-water PET and questionnaires at 3 and 6 months. The primary objective is to compare the potential benefit of early invasive coronary angiography (ICA) versus guideline directed medical therapy (GDMT) on symptomatic relief defined as freedom of angina after 3 months following a positive [15O]H2O cardiac PET/CT in patients with symptomatic chronic coronary syndrome.

Inclusion: Age > 18 years; Willing to participate and able to understand, read and sign the informed consent document before the planned procedure; Known ischemic heart disease defined as one of the following; Previous myocardial infarction, percutaneous coronary intervention or coronary artery bypass grafting; Previous coronary computed tomography angiography or invasive coronary angiography documenting atherosclerosis; Undergoing clinically indicated [15O]H2O cardiac PET/CT due to chest discomfort or dyspnea as angina equivalent; Additional inclusion criteria for randomized trial:; Initial [15O]H2O cardiac PET/CT with abnormal perfusion defined as all of the following; Hyperemic myocardial blood flow (hMBF) ≤2.3 mL/min/g in at least two adjacent myocardial segments; Relative hMBF ≤ 65% in at least two adjacent segments as compared with the mean hMBF of the two adjacent segments with the highest mean hMBF; Tissue perfusion defect extent ≥ 5% based on indices of relative hypoperfusion; Clinical indication for invasive coronary angiography decided at a multidisciplinary conference between consultants in nuclear medicine and cardiology.

Exclusion: Ongoing acute coronary syndrome or acute coronary syndrome within 30 days; Allergy to iomeron; Severe valvular disease; Very large perfusion defect on initial [15O]H2O cardiac PET/CT indicating left main coronary artery stenosis or balanced ischemia defined as tissue perfusion defect extent based on indices of absolute hMBF ≥ 20% in two or more myocardial territories supplied by coronary arteries with an Agatston calcium score ≥ 300; Contraindications for adenosine; Severe asthma; Advanced atrioventricular block without pacemaker; Severe aortic stenosis; Patients not able to breath hold (severe COPD/asthma); Pregnant women, including women who are potentially pregnant or lactating; Life expectancy of less than 2 years; Reduced kidney function with an estimated glomerular filtrations rate <40 ml/min; Inability to consent; Additional exclusion criteria for randomized trial:; Unprotected left main coronary artery stenosis on coronary CT angiography.

ClinicalTrials.gov NCT05865600