Rapid or Ultra-rapid Diagnosis of Myocardial Infarction Using High-Sensitivity Cardiac Troponin on Hospital Presentation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHerlev and Gentofte Hospital

About this trial

People with chest pain are often tested for a heart attack using a blood test called high-sensitivity cardiac troponin (hs-cTn). Traditionally, this blood test is repeated 3 hours after the first sample. Newer guidelines recommend repeating the test after 1 hour instead, which may allow patients to receive a diagnosis and leave the hospital sooner.

The purpose of the DanRUSH trial is to compare these two strategies: repeating the blood test after 1 hour versus after 3 hours in adults with suspected acute coronary syndrome. The study will evaluate whether the 1-hour strategy is as safe as the 3-hour strategy while reducing the length of hospital stay.

DanRUSH is a nationwide, pragmatic, cluster-randomized trial conducted in emergency- and cardiology departments across Denmark. The results will help determine the best timing for blood testing in patients with suspected heart attack and improve future care for these patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults (≥18 years) presenting with suspected acute coronary syndrome (ACS) with a clinical indication for high-sensitivity cardiac troponin testing

Disqualifiers

Age <18 years.

ST-segment elevation myocardial infarction (STEMI) identified on the presenting electrocardiogram and requiring immediate reperfusion therapy.

Trial design

Design model

Parallel

Treatments tested in this trial

  • 0/3-hour high-sensitivity cardiac troponin algorithm

    Diagnostic test

    High-sensitivity cardiac troponin measurements obtained at presentation and 3 hours after the initial sample as part of the conventional diagnostic strategy for suspected acute coronary syndrome.

  • 0/1-hour high-sensitivity cardiac troponin algorithm

    Diagnostic test

    High-sensitivity cardiac troponin measurements obtained at presentation and 1 hour after the initial sample as part of the accelerated diagnostic strategy for suspected acute coronary syndrome.

Treatment groups

28,000 Participants
are divided into 2 treatment groups
Group A: Conventional 0/3-hour hs-cTn AlgorithmActive comparator 1 intervention
Group B: Accelerated 0/1-hour hs-cTn AlgorithmExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Safety outcome: New myocardial infarction or cardiovascular death

The risk of new (missed or recurrent) myocardial infarction or cardiovascular death after dischage -of the 0/1-hour algorithm compared with the 0/3-hour algorithm.

Time frame
From discharge from the index hospitalization until 30 days after discharge.
2

Efficacy outcome: Length of hospital stay

Length of stay, defined as the time from presentation to the emergency department until discharge from hospital.

Time frame
During the index hospitalization (from emergency department presentation until hospital discharge)

Secondary outcomes

1

New myocardial infarction at 12 months

New myocardial infarction within 12 months following discharge from the index hospitalization, excluding myocardial infarction diagnosed during the index hospitalization.

Time frame
From discharge from the index hospitalization until 12 months after discharge.
2

All-cause mortality

Death from any cause following discharge from the index hospitalization

Time frame
30 days and 12 months following discharge
3

Overall myocardial infarction rate

Occurrence of myocardial infarction during follow-up

Time frame
30 days and 12 months following discharge
4

Diagnostic coronary angiography

Performance of diagnostic coronary angiography following the index presentation

Time frame
During the index hospitalization, at 30 days, and at 12 months after the index presentation

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Herlev and Gentofte Hospital

Lead sponsor

Bispeberg and Frederiksberg Hospital

Collaborator

Hvidovre and Amager Hospital

Collaborator

North Zealand (Hillerød) Hospital

Collaborator

Nykøbing Falster Sygehus

Collaborator

Gødstrup Hospital

Collaborator

Regionshospitalet Viborg, Skive

Collaborator

Odense Universitetshospital

Collaborator

Esbjerg sygehus

Collaborator

Aalborg University Hospital

Collaborator

This trial is not recruiting at the moment. You can still explore other options: