Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Heart heartbeats: using PEG to separate macrotroponin from real troponin elevations

Official title: HEARTBEAT-TROP. Testing of Polyethylene Glycol Precipitation to Unmask Macrotroponin in Acute Coronary Syndrome and Marathon Runners.

Run by Technical University of Munich · NCT07726420 · Data updated 2026-11-12

This study tests whether polyethylene glycol precipitation can distinguish macrotroponin from true troponin elevations in people with acute coronary syndrome and in healthy marathon runners.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment160 (estimated)
SponsorTechnical University of Munich
Academic / other
Locations1 site (Munich, Bavaria)
StatusRecruiting
StartedJuly 15, 2026
Main results expectedJuly 1, 2027
Study endsDecember 1, 2027
Registry record updatedJuly 24, 2026
Trial IDNCT07726420 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with ACS undergoing invasive coronary angiography or healthy marathon runners cleared for competition.

Probably not a fit

Patients whose troponin elevation is due to active, treatable heart disease may not benefit from PEG differentiation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In people with suspected heart events and in trained athletes, troponin can stay elevated for reasons other than acute disease. The study uses polyethylene glycol precipitation (PEG) to see if it can unmask macrotroponin and clarify troponin results. It compares ACS patients undergoing invasive coronary angiography with healthy marathon runners who have rested or just finished a race. Baseline labs and imaging are collected, and PEG and echocardiography are repeated around key time points. The primary outcome is the ability of PEG to reveal macrotroponin and differentiate it from real troponin elevation.

Why it matters

Potential benefit: If successful, PEG testing could help clinicians avoid unnecessary treatment or restrictions by correctly identifying macrotroponin.

How similar studies have gone: Previous work suggests PEG can reveal macrotroponin, but exact cut-offs are not established yet.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age above 18 years
* Group with acute coronary syndrome (ACS): Diagnosis of ACS (ST-segment elevation or non-ST-segment elevation myocardial infarction according to the European Society of Cardiology Guidelines 2023 with at least one measurement of high sensitive troponin I or T above the 99th percentile of reference).
* Marathon runners: Participation in a marathon following cardiological pre-participation screening and medical clearance for competition. No clinical signs of cardiovascular or structural heart disease

Exclusion Criteria:

* Patients with acute coronary syndrome: Known macrotroponin, terminal renal disease (glomerular filtration rate below 10ml per minute), diagnosis of cancer, pregnancy
* Marathon runners: Coronary artery disease, structural heart disease, diagnosis of cancer, pregnancy

Where it's running

  • Technical University Munich
    Munich, Bavaria, Germany
    Recruiting

Study contacts

  • Principal investigator: Simon Wernhart, MD, PhD — TUM - Technische Universität München
  • Study coordinator: Simon Wernhart, MD, PhD
  • Email: simon.wernhart@gmx.de
  • Phone: +491751830099

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.