At a glance
ClinicalIndex Comparison RecordN/ACompleted· 55 enrolled
Drug / intervention
Insertable Cardiac Monitordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Hybrid Ablation Plus Medical Therapy for Persistent Atrial Fibrillation (HYBRID AF)
In Brief
A clinical study evaluating Insertable Cardiac Monitor for Persistent Atrial Fibrillation. Completed, enrolled 55 participants across 4 sites.
Detailed Summary
This clinical trial is designed to compare two management strategies for the treatment of asymptomatic/subclinical atrial fibrillation after ablation based on data from the Biotronik ICM (BioMonitor3® or future generation of Biotronik ICM).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPersistent Atrial Fibrillation
CountriesUnited States
CollaboratorsBiotronik, Inc.
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedDec 2019
Enrollment StartJun 2020
Primary CompletionFeb 2024
TodayJul 2026
First PostedDec 9, 2019
Enrollment StartJun 25, 2020
Primary CompletionFeb 15, 2024
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 6.6 years ago
Interventions
Insertable Cardiac Monitordevice
Implantable device that provides accurate daily transmission of cardiac electrical data for arrhythmia detection.