Skip to content

CT Coronary Angiography for Type 2 Myocardial Infarction

A Pilot Clinical Trial of CT Coronary Angiography for Patients With Suspected Type 2 Myocardial Infarction

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06047392
Enrollment
100
Registered
2023-09-21
Start date
2023-07-24
Completion date
2025-02-28
Last updated
2023-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction, Coronary Artery Disease

Keywords

Computed Tomography, Myocardial Infarction, Coronary Artery Disease

Brief summary

This study is to explore whether a computed tomography (CT) scan of the heart arteries might improve the care of patients that have presented with a suspected Type 2 myocardial infarction (MI). The Investigators hope to demonstrate that these patients may be the ideal group of patients to benefit from cardiac CT scan imaging by; 1. confirming whether they have any disease in their heart arteries 2. demonstrating the severity of the heart artery disease 3. revealing an alternative cause for their presentation 4. avoiding the need for an invasive heart artery angiogram.

Detailed description

An increasing number of patients present to hospital with a heart attack (myocardial infarction, MI). Heart attacks can be caused by instability and narrowing in heart arteries (Type 1 MI) or strain on the heart (Type 2 MI). Type 2 MIs can be the result of other problems with the heart including inflammation and rhythm problems or other conditions such as infection or low blood count. Both Type 1 and Type 2 MI patients have increased risk of further problems following this presentation. Deciding whether a patient has suffered a Type 1 MI or a Type 2 MI can be very difficult leaving uncertainty for patients and health care staff. Often patients with Type 2 myocardial infarction are either referred for an invasive coronary angiogram (a procedure where dye is injected into the heart arteries directly) or have no further investigations. Invasive angiograms carry a small risk of complications including heart attack, stroke and, rarely, death. Cardiac CT scanning has emerged in the last 20 years as the first test usually performed to investigate patients that present with stable chest pain symptoms to the outpatient department. The role of cardiac CT in patients that present as an emergency with a suspected heart attack is not yet established. To date, there are no substantive data on the role of computed tomography coronary angiography (CTCA) in patients with known or suspected Type 2 MI. A pilot study is proposed to address the information gaps. The specific areas of uncertainty include feasibility of enrolling into an imaging trial during acute medical care, feasibility of randomisation (including compliance and cross-overs), incremental diagnostic value, safety (procedure and post-procedure) and healthcare resource utilisation. The study aims to address the gap in evidence highlighted by the recent European Society of Cardiology Guidelines for the management of acute coronary syndromes, 'evaluating diagnostic strategies to better classify patients according to their type of MI (Type 1 vs Type 2)'.

Interventions

Patients will undergo a CTCA according to local, standard protocol.

Sponsors

University of Glasgow
CollaboratorOTHER
British Heart Foundation
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with known or suspected Type 2 MI

Exclusion criteria

1. Unable to provide written informed consent 2. Known severe coronary artery disease 3. Previous PCI 4. Previous CABG 5. Severe renal dysfunction, defined as an eGFR \<30 mL/min/1.73 m2 6. Tachycardia (\>75bpm) refractory to heart rate control 7. Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Change in primary diagnosisAt discharge from recruiting hospital (assessed up to day 30)The primary outcome is a change in the primary diagnosis defined as a difference in the final diagnosis at discharge compared to the initial diagnosis prior to study recruitment. The primary outcome will therefore take account of the diagnostic effect of CTCA and any changes that might normally occur during standard care.

Secondary

MeasureTime frameDescription
Functional assessment6 monthsDuke Activity Status Index (DASI). Range 0 - 58.2. Higher score indicates better functional status.
Rate of invasive coronary angiography3 monthsPatients undergoing invasive coronary angiography following presentation
Major adverse cardiovascular events12 monthsMyocardial infarction, stroke or death
Health related quality of life assessment6 monthsEQ-5D-5L questionnaire. Reported as 5 digit code (Range 11111 - 55555) with higher numbers indicating worse quality of life and EQ visual analogue scale (Range 0-100) with higher numbers indicating better quality of life.
Rate of hospital readmission12 monthsReadmission to hospital for any reason
Rate of additional cardiovascular investigations12 monthsReferral to outpatient clinic or for additional cardiovascular test (including exercise tolerance testing, echocardiography, myocardial perfusion imaging, cardiac MRI)
Estimated cost of health care12 monthsHealth care resource utilisation including length of hospital stay, investigations and treatment
Rate of coronary revascularisation12 monthsEither percutaneous coronary intervention or coronary artery bypass grafting

Countries

United Kingdom

Contacts

Primary ContactMaureen Travers
maureen.travers@ggc.scot.nhs.uk+44141 314 4012

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026