At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 1,300 enrolled
Drug / intervention
Pacemaker Medtronic EnRhythmdevice
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.
MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and Heart Failure
In Brief
A Phase 4 clinical trial evaluating Pacemaker Medtronic EnRhythm for Atrial Fibrillation and Heart Failure, Congestive. Completed, enrolled 1,300 participants across 1 site.
Detailed Summary
The aim of this study is to test the impact of the managed ventricular pacing (MVP) mode and atrial preventive and antitachycardia pacing therapies on the reduction of a composite clinical outcome composed of any death, permanent atrial fibrillation, and cardiovascular hospitalizations.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAtrial Fibrillation, Heart Failure, Congestive
CountriesItaly
Collaborators--
Timeline
Phase 4CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 2005
Enrollment StartFeb 2006
Primary CompletionApr 2012
Study CompletionApr 2013
TodayJul 2026
First PostedDec 6, 2005
Enrollment StartFeb 1, 2006
Primary CompletionApr 1, 2012
Study CompletionApr 1, 2013
TodayJul 2, 2026
Enrollment to primary: 6.2 yearsPosted 20.6 years ago
Interventions
Pacemaker Medtronic EnRhythmdevice
Pacemaker specific programming