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

Sponsor: London North West Healthcare NHS Trust

NCT ID: NCT06185530

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Detection of obstructive coronary disease (diagnostic test)
How long the study runs
Study runs about 99 months (dates as stated)
About the drug or intervention
Detection of obstructive coronary disease — diagnostic test: Detection of obstructive coronary disease
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
2,000
Started
2023-09-18
Last checked
2025-10

Plain English Summary

What is this study?

  • • Testing a new treatment for chronic coronary syndrome
  • • NA - 2,000 participants
  • • Diseases of the heart and circulation are known as cardiovascular diseases, and they cause over 160,000 deaths each year

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with chronic coronary syndrome

Where?

  • • Harrow - London North West University Healthcare NHS Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Chronic Coronary SyndromeCoronary DiseaseCoronary Artery Disease

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

eGFR

Treatment history

Treatments you must have had:

  • ✓ a further imaging investigation, either SE or CTCA, to evaluate a suspected diagnosis of CAD

What the study is looking for

  • ✓Age \> 18 years old
  • ✓Patients referred to RACPC and judged by the reviewer to require a further imaging investigation, either SE or CTCA,...
  • ✓Have a PTP score ≥ 5%, as calculated using ESC guidelines OR
  • ✓i) Constricting symptoms in the front of the chest or in the neck, jaw, shoulder or arm ii) Precipitated by physical...
  • ✓Able to give agreement to take part to participate in the study and its follow up

Who cannot take part

  • ✗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%...
  • ✗Patients who have undergone invasive or non-invasive, functional or anatomical (Including CAC score) testing for...
  • ✗Documented allergy to iodinated contrast or documented allergy to both ultrasound contrasts used at LNWH Trust;...
  • ✗Contraindications to undergoing CTCA, including but not limited to;
See the full criteria
Inclusion Criteria: 1. Age \> 18 years old 2. 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 3. AND 1. Have a PTP score ≥ 5%, as calculated using ESC guidelines OR 2. 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 4. Able to give informed consent to participate in the study and its follow up Exclusion Criteria: 1. Patients with diagnosed ACS that require urgent or emergency treatment or hospitalisation for inpatient investigations. 2. Known history of obstructive CAD (Previous MI, PCI or CABG) or previous invasive angiography with evidence of ≥ 50% stenosis in any epicardial vessel. 3. 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. 4. 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 5. 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 6. 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) 7. Known pregnancy 8. Unable to provide informed consent

Where Is This Study? (1 UK site)

London North West University Healthcare NHS Trust

Harrow HA1 3UJ, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Emma Howard

Sponsor contact

CONTACT

0208 869 2548 emma.howard16@nhs.net
Data sourced from ClinicalTrials.gov · Last verified: 2025-10