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Study identifier: NCT06920030 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Performance of the Cardiac Microcurrent (C-MIC) System With a Less Invasively Placed Left Ventricular Lead

Condition: Idiopathic Cardiomyopathy · Left Ventricular (LV) Systolic Dysfunction · Non-ischemic Cardiomyopathy  ·  Sponsor: Berlin Heals GmbH

PhaseNA
Planned participants22
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Patients with idiopathic dilated cardiomyopathy in heart failure (NYHA class III - IV) with a baseline left ventricular ejection fraction between ≥25% and ≤35%, and patients with non-ischemic cardiomyopathy in heart failure (NYHA class III-IV) with a baseline left ventricular ejection fraction \>40% and \<50% despite guideline-directed medical therapy, will receive C-MIC treatment in addition to optimal medical management. The device can be implanted without the need for open-heart surgery. Patients are assigned to one of two groups according to the indications under investigation. At the end of the study after 6 months, the C-MIC System will be turned off. The primary endpoint of the study is the absolute change in left ventricular ejection fraction after 6 months of treatment.

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

Talk to the study team

Susanne Becker  ·  +49 308891364053  ·  becker@berlinheals.de

John Brumfield  ·  +49 308891364053  ·  brumfield@berlinheals.de

Always discuss trial participation with your own doctor first.

Locations (4)

University Clinical Center of the Republic of SrbskaBanja Luka, Republic of Srbska, Bosnia and HerzegovinaRecruiting
Institute of Cardiovascular Disease DedinjeBelgrade, SerbiaRecruiting
Clinical Hospital Center Bezanijska kosaBelgrade, SerbiaRecruiting
UKC KragujevacKragujevac, SerbiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06920030