Clinical Trials
5
Trial Phases
2 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
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Clinical Trials
Distribution across different clinical trial phases (5 trials with phase data)• Click on a phase to view related trials
Performance of the Cardiac Microcurrent (C-MIC) System With a Less Invasively Placed Left Ventricular Lead
- Conditions
- Idiopathic CardiomyopathyLeft Ventricular (LV) Systolic Dysfunction
- First Posted Date
- 2025-04-09
- Last Posted Date
- 2025-04-27
- Lead Sponsor
- Berlin Heals GmbH
- Target Recruit Count
- 33
- Registration Number
- NCT06920030
- Locations
- 🇧🇦
University Clinical Center of the Republic of Srbska, Banja Luka, Republic of Srbska, Bosnia and Herzegovina
🇷🇸Institute of Cardiovascular Disease Dedinje, Belgrade, Serbia
The C-MIC-II Follow-Up Study
- Conditions
- Systolic Left Ventricular Dysfunction
- First Posted Date
- 2022-01-13
- Last Posted Date
- 2025-06-08
- Lead Sponsor
- Berlin Heals GmbH
- Target Recruit Count
- 31
- Registration Number
- NCT05189860
- Locations
- 🇲🇰
University Clinic Cardiac Surgery, Skopje, North Macedonia
🇧🇦University Clinical Centre of Republic of Srpska, Banja Luka, Bosnia and Herzegovina
🇧🇦University Clinical Center of Sarajevo, Sarajevo, Bosnia and Herzegovina
Performance and Safety of the Cardiac Microcurrent Therapy System
- Conditions
- Systolic Left Ventricular Dysfunction
- Interventions
- Device: CMICDrug: Standard of Care (SOC)
- First Posted Date
- 2020-12-10
- Last Posted Date
- 2025-04-02
- Lead Sponsor
- Berlin Heals GmbH
- Target Recruit Count
- 70
- Registration Number
- NCT04662034
- Locations
- 🇧🇦
University Clinic, Banja Luka, Bosnia and Herzegovina
🇧🇦University Clinic Sarajevo, Sarajevo, Bosnia and Herzegovina
🇧🇬Diagnostic and Consultative Center Neoclinic Ead, Sofia, Bulgaria
News
C-MIC II Trial Shows Microcurrent Therapy Significantly Improves Heart Function in Heart Failure Patients
The C-MIC II randomized controlled trial demonstrated that microcurrent therapy significantly improved left ventricular ejection fraction by 5.1% compared to controls in heart failure patients with reduced ejection fraction.
