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Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Procedures

NCT00288288 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2012-09-25

No results posted yet for this study

Summary

The primary purpose of this study is to compare the time, risk and cost savings of 2 patient groups who receive FDA approved left ventricular pacing leads.

Conditions

Interventions

PROCEDURE

Epicardial left ventricular lead placement

Epicardial left ventricular lead placement

PROCEDURE

Transvenous left ventricular lead implant

Transvenous left ventricular lead implant

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • University of Kansas

    lead OTHER

Principal Investigators

  • Loren Berenbom, MD · University of Kansas Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Completion
2010-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT00288288 on ClinicalTrials.gov