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A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurations

NCT01032577 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-02-28

No results posted yet for this study

Summary

The PropR study will evaluate sensing during ventricular fibrillation (VF) in both bipolar and extended bipolar configurations, in order to evaluate if both can be used interchangeably in caring for patients. In addition, follow up evaluation of R wave amplitude over time would allow us to determine whether one configuration is more likely to be associated with change. This understanding would be important in selecting the proper configuration at the time of implant.

Conditions

  • Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Trinity Health Of New England

    lead OTHER

Principal Investigators

  • Aneesh Tolat, MD · Attending Cardiac Electrophysiologist, St Francis Hospital and Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2011-07-31
Completion
2011-07-31

Countries

  • United States

Study Locations

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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 NCT01032577 on ClinicalTrials.gov