Suspended

A Randomized, Prospective Multicenter Study to Determine the Incidence of Atrial Fibrillation and Heart Failure in Correlation to Stimulation Modes of Pacemakers

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What is being tested

Data Collection

Who is being recruted

Cardiac Conduction System Disease+8

+ Arrhythmias, Cardiac

+ Arrhythmia, Sinus

Over 18 Years
+25 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Phase 4
Interventional
Study Start: November 2004
See protocol details

Summary

Principal SponsorMedtronic BRC
Study ContactMatthias Reimers, Dipl. DocumentalistMore contacts
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 1, 2004

Actual date on which the first participant was enrolled.

Background: Dual-chamber pacemaker therapy has become the mainstay for treating symptomatic sick sinus syndrome (SSS). This approach aims to results in a physiologic conduction pattern, while protecting against atrioventricular conduction anomalies. Smaller studies and subgroup analyses of larger trials suggest that ventricular stimulation associated with this treatment has adverse effects, especially an increased incidence of atrial fibrillation and heart failure. Methods: In MODEST, a study on patients with sick sinus syndrome who have an indication for pacing therapy, atrial pacing (AAI) is compared with dual-chamber pacing (DDD) combined with a novel algorithm developed to lower the number of ventricularly paced beats. The study aims to assess the impact of ventricular pacing on the development of atrial arrhythmias and to test the hypothesis that DDD pacing using the algorithm is associated with a higher rate of atrial arrhythmias as atrial pacing. Included will be patients with SSS and no high degree AV node disease except for patients with first-degree AV block ≤300ms. Patients will be followed stratified by their Wenckebach point (≥ 120 bpm versus < 120 bpm). Conclusion: MODEST is a large, prospective, randomized, multicenter trial aiming to compare a novel type of dual-chamber pacing approach (that includes an algorithm designed to lower the number of ventricularly paced beats) with pure atrial pacing, assessing the impact on the incidence of atrial arrhythmias in patients with sick sinus syndrome.

Official TitleA Randomized, Prospective Multicenter Study to Determine the Incidence of Atrial Fibrillation and Heart Failure in Correlation to Stimulation Modes of Pacemakers
NCT00161551
Principal SponsorMedtronic BRC
Study ContactMatthias Reimers, Dipl. DocumentalistMore contacts
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

402 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiac Conduction System DiseaseArrhythmias, CardiacArrhythmia, SinusAtrial FibrillationCardiovascular DiseasesHeart BlockHeart DiseasesHeart FailurePathologic ProcessesSick Sinus SyndromePathological Conditions, Signs and Symptoms

Criteria

4 inclusion criteria required to participate
Symptomatic sinus bradycardia, Sinusarrest

Symptomatic SA block

Bradycardia-Tachycardia-Syndrome

Binodal diseases

21 exclusion criteria prevent from participating
1st degree AV Block

2nd degree AV block

3rd degree AV block

Total right bundle branch block

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 5 locations

Recruiting

Klinikum Coburg

Coburg, GermanyOpen Klinikum Coburg in Google Maps
Recruiting

Universitätskrankenhaus Eppendorf

Hamburg, Germany
Recruiting

Kardiologische Gemeinschaftspraxis

Papenburg, Germany
Recruiting

Kardiologische Praxis

Starnberg-Percha, Germany
Suspended5 Study Centers