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CArdiac cT in the Treatment of Acute CHest Pain 2 - Myocardial CT Perfusion

Myocardial Perfusion 320 MDCT Guided Treatment Strategy for the Clinical Management of Patient With Recent Acute-onset Chest Pain. A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02014311
Acronym
CATCH2
Enrollment
600
Registered
2013-12-18
Start date
2013-10-31
Completion date
2022-12-31
Last updated
2022-12-12

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

Conditions

Coronary Artery Disease

Keywords

Multidetector Computed Tomography, Myocardial Perfusion Imaging, Coronary Stenosis, Coronary Artery Disease, Angina Pectoris

Brief summary

The aim of this study is to assess whether the clinical management of patients with recent acute-onset chest pain without acute coronary syndrome may be optimized by a combined coronary CT angiography (CTA) + CT myocardial perfusion (CTP) guided, rapid diagnostic strategy as compared to CTA alone. CT diagnostic evaluation and potential referral for invasive testing will be performed within 2 weeks after hospital discharge. The following main hypothesis will be tested: \- Combined assessment of coronary anatomy and myocardial perfusion using 320 MDCT results in a safe and optimized, cost-effective invasive treatment strategy

Detailed description

MATERIAL \- Consecutive patients referred with chest pain in whom acute coronary syndrome has been excluded, yet with a maintained clinical suspicion of coronary artery disease will be included in the study. Only patients deemed clinically suited for subsequent invasive evaluation and treatment will be included. METHODS -If the patients accept participation in the trial a computerized 1:1 randomization for CTA alone (control group) or CTA and CTP combined (intervention group) within 2 weeks from discharge will be conducted. CT angiography and CT myocardial perfusion imaging will be performed using a 320-slice MSCT Toshiba VISION Edition Aquilion One scanner according to recommendations from the vendor and clinical routine developed at Rigshospitalet. Based on CTA and/or CTP findings patients will be referred for invasive evaluation including fractional flow reserve assessment (FFR) and treatment within 30 days. Invasive procedures will be performed according to international guidelines and the frequency of revascularization procedures recorded. Clinical outcome data according to specified secondary endpoints will be recorded from hospital charts and medical registries.

Interventions

PROCEDURECTA+CTP guided treatment strategy

CTA+CTP guided treatment strategy

PROCEDURECTA guided treatment strategy

CTA guided treatment strategy

Sponsors

Copenhagen University Hospital, Hvidovre
CollaboratorOTHER
Amager Hospital
CollaboratorOTHER
Bispebjerg Hospital
CollaboratorOTHER
Herlev Hospital
CollaboratorOTHER
Glostrup University Hospital, Copenhagen
CollaboratorOTHER
University Hospital, Gentofte, Copenhagen
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Recent acute-onset chest pain where coronary artery disease is suspected * During initial acute hospitalization: 1. Normal coronary biomarkers (Troponins) 2. No or non-diagnostic ECG changes (LV hypertrophy, bundle branch blok, pacemaker rhythm) * Age ≥50 years * ≥ 1 cardiovascular risk factor (family history of CAD, hypertension, hypercholesterolemia, diabetes, smoking) corresponding to a Duke clinical score ≥20%

Exclusion criteria

* Known Iodine contrast allergy * Estimated GFR below 50 ml/min * Adenosine intolerance - known allergic asthma * Previous CABG * Patient related circumstances which preclude informed consent from the patient * Patients in whom psychiatric, physical or geographic conditions do not allow long-term clinical followup * Expected survival of less that 2 years

Design outcomes

Primary

MeasureTime frameDescription
Frequency of coronary revascularization among included patients referred for invasive investigationWithin 60 days of study inclusionAmong patients referred for invasive coronary evaluation the frequency of subsequent PCI and/or CABG is recorded

Secondary

MeasureTime frameDescription
Hospital admittance due to recurrence of chest pain, acute myocardial infarction or cardiac deathWithin 3, 12 and 24 months after CT examination
New referral for invasive investigation following inititial evaluation3, 12 and 24 months after CT examination
Coronary revascularization - not including revascularization related to index evaluation3, 12 and 24 months after CT examination
Invasive procedure related eventsWithin 30 days of invasive procedureAmong patients referred for invasive evaluation and treatment, procedure related events including death, bleeding, vascular complications, stroke and acute myocardial infarction will be recorded

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026