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Clinical Trials/NCT00262119
NCT00262119
Completed
Phase 4

MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and Heart Failure

Medtronic Cardiac Rhythm and Heart Failure1 site in 1 country1,300 target enrollmentFebruary 1, 2006

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
Medtronic Cardiac Rhythm and Heart Failure
Enrollment
1300
Locations
1
Primary Endpoint
Composite Endpoint Composed by Death for Any Cause, Cardiovascular Hospitalization or Permanent AF at 2 Years
Status
Completed
Last Updated
10 months ago

Overview

Brief 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.

Detailed Description

Kristensen et al. reported that AAIR pacing reduces atrial fibrillation (AF) development compared to DDDR pacing in sinus node disfunction patients. Several authors have shown that, in patients with intact AV conduction, unnecessary chronic RV pacing can cause detrimental effects such as AF, left ventricular (LV) dysfunction and congestive heart failure. These findings arose the hypothesis that the non-physiologic nature of ventricular pacing may result in electrophysiological and LV remodeling changes that have potentially deleterious long-term effects. The MVP mode, present in the Medtronic pacemaker EnRhythm, provides atrial based pacing with ventricular backup. It operates in true AAI(R) mode, it provides ventricular backup in case of a single conduction loss and converts to DDD(R) mode in case of persistent loss of AV conduction. Aim of this study is to test the impact of the MVP pacing mode and atrial preventive and antitachycardia pacing therapies on the reduction of a composite clinical outcome composed by any death, permanent AF, cardiovascular hospitalizations.

Registry
clinicaltrials.gov
Start Date
February 1, 2006
End Date
April 1, 2013
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medtronic Cardiac Rhythm and Heart Failure
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Class I/Class II indications for dual chamber pacing
  • Previous implant of an EnRhythm dual chamber implantable pulse generator (IPG) since maximum 2 weeks
  • History of atrial arrhythmias (at least one electrocardiogram \[ECG\] or Holter documented episodes in the last 12 months)

Exclusion Criteria

  • Less than 18 years of age
  • Pregnancy
  • Unwilling or unable to give informed consent or to commit to follow-up schedule
  • Medical conditions that preclude protocol required testing or limit study participation
  • Enrolled or intend to participate in another clinical trial during the course of this study
  • A life expectancy of less than 2 years
  • Patient is a candidate for an implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy (CRT) device implant
  • Anticipated major cardiac surgery within the course of this study
  • Permanent III degree AV-block or history of AV node ablation
  • History of permanent AF (as defined below)

Outcomes

Primary Outcomes

Composite Endpoint Composed by Death for Any Cause, Cardiovascular Hospitalization or Permanent AF at 2 Years

Time Frame: 2 years

The outcome measurement is the 2 years incidence, calculated by Kaplan Meier survival analysis, of the composite endpoint composed by death for any cause, cardiovascular hospitalization or permanent AF.

Secondary Outcomes

  • Incidence of Permanent Atrial Fibrillation at 2 Years(2 years)
  • Burden of Composite Clinical Endpoint(2 years)
  • Cardiovascular Death(2 years)
  • Clinical Outcome in All the Patients With MVP ON Between Patients With Optimized AV-delay and Patients Without Optimized AV-delay(2 years)
  • Subjects' Symptoms(2 years)
  • Heart Failure Medications(2 years)
  • Any Hospitalization(2 years)
  • Adverse Events(2 years)
  • Development of Atrioventricular (AV) Block and Pacemaker Dependency(2 years)
  • Predictors of Stroke, Transient Ischemic Attack (TIA) and Arterial Embolism(2 years)
  • Incidence of Cardiovascular Hospitalizations at 2 Years(2 years)
  • Persistent Atrial Fibrillation (AF)(2 years)
  • Echocardiogram Data About Left Ventricular Fractional Shortening and Ejection Fraction and Left Atrium Dilatation(2 years)
  • Death for All Causes at 2 Years(2 years)
  • Cumulative Percentage of Ventricular Pacing(2 years)
  • Atrial Fibrillation Burden(2 years)
  • Time to Development of the Composite Endpoint Between All Randomized Subjects in the Three Arms in Subgroups of Patients(2 years)
  • Frequency, Type, and Associated Cost of Health Care Utilization and Utility(2 years)

Study Sites (1)

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