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Study identifier: NCT05326828 Synced from ClinicalTrials.gov · July 28, 2026
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Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINOCA

Condition: MINOCA · Atrial Fibrillation  ·  Sponsor: Insel Gruppe AG, University Hospital Bern

PhaseN/A
Planned participants60
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

Myocardial infarction with non-obstructive coronary arteries (MINOCA) (i.e.\<50% stenoses) on coronary angiography) is an underappreciated clinical entity concerning 5-6% of patients with acute myocardial infarction. Approximately 50% of these patients remain without appropriate diagnosis and treatment. The MINOCA study aims at systematically assessing the frequency of underlying pathologies of MINOCA and outcomes with a multidisciplinary etiologic work-up and follow-up of 5 years including, for the first time, an implantable cardiac monitor (ICM) to assess the frequency of atrial fibrillation as underlying cause for MINOCA.

This description comes directly from the study's public registry record.

Talk to the study team

Lorenz Räber, MD, PhD  ·  +41 31 632 50 00  ·  lorenz.raeber@insel.ch

Sarah Bär, MD  ·  sarah.baer@insel.ch

Always discuss trial participation with your own doctor first.

Locations (2)

Bern University Hospital InselspitalBern, SwitzerlandRecruiting
University Hospital Zurich USZZurich, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT05326828