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Quadripolar Pacing Post Approval Study

NCT01555619 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1971

Last updated 2019-04-16

No results posted yet for this study

Summary

The purpose of this post-approval study is to evaluate the acute and chronic performance of a Quadripolar CRT-D device system in a patient population indicated for cardiac resynchronization therapy (CRT).

Conditions

Interventions

DEVICE

CRT-D System

Implantation of a CRT-D System

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Raffaele Corbisiero, MD · Deborah Heart and Lung Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-15
Primary Completion
2019-02-28
Completion
2019-02-28
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01555619 on ClinicalTrials.gov