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Biventricular Alternative Pacing | Clinical Trials | Clareo Health

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WITHDRAWNPhase 4NCT00559143

Biventricular Alternative Pacing

Aim of present study is to examine the short and long-term results of pacing from right ventricular apex and to compare them with those of biventricular pacing.

Lead sponsor: Medtronic Hellas Medical Devices ΑEE•1 locations•View source on ClinicalTrials.gov

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What this study is about

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Sponsors

Lead Sponsor

Medtronic Hellas Medical Devices ΑEE

In this study all subjects to be studied will have atrioventricular conduction disturbances that require permanent artificial pacing. In all subjects a biventricular pacemaker will be implanted. Moreover the subjects will be randomized in a biventricular or conventional pacing mode and will be observed for a long term period.

Age

18 - 75 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Subjects between the age of 18 to 75 years with classic indication for permanent artificial pacing in which it is expected very high percentage of ventricular pacing, (pacing systoles constitute the 80% and more of the total).
•Physiologic or mildly affected systolic function of left ventricle, LVEF\> 40%.
•Subject is willing and able to comply with the Clinical Investigational Plan and to remain available for follow-up visits, through study closure.
•Subject (or if allowed by local law/regulations: subject's legally authorised representative) is willing and able to sign and date the study Informed Consent.

Exclusion Criteria

•Subjects with classic indication for Biventricular Pacing - (European Guidelines 2007).
•Permanent atrial fibrillation.
•Cardiovascular surgery within the last three months prior to enrollment.
•Myocardial infarction within the last three months prior to enrollment.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 8, 2011Terms

Trial snapshot

StatusWITHDRAWN

PhasePHASE4

Enrollment38

Start dateNov 2007

Last updatedJun 8, 2011

Condition

Atrioventricular Block

Locations shown

University Hospital of Crete

Heraklion, Crete

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 8, 2011Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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