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MADIT-CRT LONG-TERM INTERNATIONAL FOLLOW-UP REGISTRY - EUROPE

NCT02060110 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 447

Last updated 2014-02-11

No results posted yet for this study

Summary

The registry is designed to determine the long-term mortality and morbidity benefit as a result of Cardiac Resynchronization Therapy with Defibrillation (CRT-D) vs. Implantable Cardioverter Defibrillator (ICD) therapy in the MADIT-CRT study patient population. The registry will collect data on patients that previously participated at MADIT-CRT sites within Europe through five years of participation from their orginal enrollment in the MADIT-CRT IDE study.

Conditions

Interventions

DEVICE

Patients that were randomized to the the cardiac resynchronization therapy with defibrillation (CRT-D) device for the study

DEVICE

MADIT-CRT ICD ONLY ARM

Sponsors & Collaborators

  • Israeli Association for Cardiovascular Trials - IACT

    collaborator UNKNOWN

  • Sheba Medical Center

    lead OTHER_GOV

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2013-09-30
Completion
2014-01-31

Countries

  • Israel

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 NCT02060110 on ClinicalTrials.gov