OPTIMA Bi-ventricular Capture Verification Study

NCT00887055 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2015-06-29

No results posted yet for this study

Summary

The purpose of this study is to characterize the morphology (shape) of the intracardiac electrograms(EGM) from patients with a resynchronization therapy device.

Conditions

Interventions

DEVICE

CRT device

Sponsors & Collaborators

  • Guidant Corporation

    lead INDUSTRY

Principal Investigators

  • Francois Philippon, MD · Hopital Laval, 2725 Chemin Ste-Foy, Ste-Foy, Quebec, Canada G1V 4G5 418-656-8711

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • Canada

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00887055 on ClinicalTrials.gov