SECURE Trial: Stress Echocardiography With Carotid Ultrasound vs Routine CT Coronary Angiography in Chronic Coronary Syndrome for Endpoints

Official title

Stress Echocardiography With Carotid Ultrasound vs Routine CT Coronary Angiography in Suspected Chronic Coronary Syndrome for the Detection of Obstructive Coronary Disease and Prevention of Adverse Outcomes.

Overview

Diseases of the heart and circulation are known as cardiovascular diseases, and they cause over 160,000 deaths each year. Coronary heart disease (CHD) is the most common cardiovascular disease. This is due to a build-up of fatty material, known as atherosclerosis, in the blood vessels supplying blood to the heart muscle. This can cause chest pain or if blocked, can cause a heart attack. Two of the main non-invasive tests to look for coronary heart disease are Computed Tomography Coronary Angiography (CTCA) and Stress Echocardiography (Ultrasound scan). CTCA shows the arteries and allows small amounts of disease to be seen that may not yet be causing any symptoms. However, if there's lots of disease and calcification, it becomes difficult to tell how severe it is, which means several tests may be needed. Stress Echocardiography shows if enough blood is reaching the heart muscle, so can show if there is severe disease that needs treatment. However, it can't see the arteries so doesn't showt small disease that may benefit from tablet treatment. There is not yet an effective non-invasive combined test that can give all this information in one go. Studies have shown that if there's atherosclerosis in another artery, a person is very likely to have coronary atherosclerosis as well. Carotid atherosclerosis, in the neck arteries, can be seen with ultrasound similar to stress echocardiography. So, by combining these two tests the investigators want to see if it is possible to see severe as well as small areas of disease in one test, to provide better treatment. The study will enrol 2,000 participants, who need investigation for CHD, equally randomised to CTCA or stress echocardiography with carotid ultrasound. We will follow these participants for 5 years and observe for any adverse outcomes and ask them to complete a questionnaire.

Interventions

• Diagnostic test Detection of obstructive coronary disease
  Detection of obstructive coronary disease

Primary outcome measures

• Detection of obstructive CAD and prevalence of MACE in enrolled participants [Time frame: Within 3 months of randomisation confirmed by documentation in medical record]

Secondary outcome measures (6)

• Assessment of resource utilisation between study arms (subsequent downstream testing, cardiac related hospital visits, costs and incremental cost effectiveness) [Time frame: Time to first event, up to 18 months post randomisation, confirmed by medical record documentation]
• Assessment of overall ionising radiation exposure (dose) between study arms [Time frame: Within 3 months of randomisation, confirmed by documentation in investigation report]
• Major complications from cardiovascular procedures or cardiovascular diagnostic testing [Time frame: Up to18 months from randomisation to time of first documented outcome in medical records]
• Analysis of patient derived chest pain related quality of life (EQ-5D) [Time frame: at 6-months and 12-months after randomisation on telephonecall questionnaire completion with patient]
• Change in prescription of preventative therapies (including statin and anti-platelet agents or dose increase of current statin therapy > 50%) [Time frame: Up to 18 months from randomisation to time of first documented outcome in medical records]
• The proportion of patients undergoing invasive coronary angiography and revascularisation, of the target lesion, either through PCI or CABG, at follow up. [Time frame: Time (in days) from the initial investigation until revascularisation confirmed by medical record documentation]

Eligibility criteria

Inclusion criteria

• Age > 18 years old
• Patients referred to RACPC and judged by the reviewer to require a further imaging investigation, either SE or CTCA, to evaluate a suspected diagnosis of CAD
• AND

• Have a PTP score ≥ 5%, as calculated using ESC guidelines OR
• Have clinical history in keeping with 'typical' angina symptoms, as judged by the investigator, in patients with a PTP score <5% - With 'typical' symptoms, as per ESC guidelines, being all three of the following

i) Constricting symptoms in the front of the chest or in the neck, jaw, shoulder or arm ii) Precipitated by physical exertion iii) Relieved by rest or nitrates within 5 minutes

• Able to give informed consent to participate in the study and its follow up

Exclusion criteria

• Patients with diagnosed ACS that require urgent or emergency treatment or hospitalisation for inpatient investigations.
• Known history of obstructive CAD (Previous MI, PCI or CABG) or previous invasive angiography with evidence of ≥ 50% stenosis in any epicardial vessel.
• Patients who have undergone invasive or non-invasive, functional or anatomical (Including CAC score) testing for detection of CAD within the previous 1 year of clinical assessment.
• Documented allergy to iodinated contrast or documented allergy to both ultrasound contrasts used at LNWH Trust; Luminity® (Perflutren) and SonoVue® (Sulphur Hexafluoride) or the constitutes
• Contraindications to undergoing CTCA, including but not limited to;

• eGFR < 40 ml/min
• Contraindications to beta-blockers including but not limited to, documented allergy or significant airways disease in the judgement of the investigator.
• Exceeding CT scanner weight tolerance
• Contraindications to undergoing SE, including but not limited to;

• Known cardiomyopathic process (Hypertrophic cardiomyopathy (HCM)) with resting gradient > 50mmHg or severe valvular lesion
• Severe uncontrolled hypertension (≥180/100mmHg)
• Known pregnancy
• Unable to provide informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Diagnostic

Study locations

United Kingdom · 1 center

• London North West University Healthcare NHS Trust — Harrow

Identifiers

NCT: NCT06185530 · CRC/2023/001

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗