SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac Resynchronization Therapy Defibrillator Patients

NCT00940888 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1701

Last updated 2019-02-04

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to characterize the chronic performance of the St. Jude Medical SJ4 connector and RV high voltage SJ4 leads.

Conditions

Interventions

DEVICE

SJ4 connector and RV high voltage SJ4 lead

Standard of care implantation of SJ4 device system

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Bruce Wilkoff, MD · The Clevleland Clinic Foundation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2015-09-30
Completion
2015-12-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT00940888 on ClinicalTrials.gov