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Cardiac Resynchronization Therapy Modular Registry

NCT01573091 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2017-02-24

No results posted yet for this study

Summary

The purpose of the study is to collect some parameters (clinical, electrical, radiographic, echocardiographic and ECG) able to predict response to cardiac resynchronization therapy.

Conditions

Interventions

PROCEDURE

Cardiac Resynchronization Therapy

Any commercially available Cardiac Resynchronization Therapy devices with or without defibrillation backup (CRT-D/CRT-P) can be used upon discretion of the investigator according to current guidelines

Sponsors & Collaborators

  • Giuseppe Ricciardi

    lead OTHER

Principal Investigators

  • Luigi Padeletti, MD · Department of Heart and Vessels, University of Florence, Florence, Italy.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • Italy

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 NCT01573091 on ClinicalTrials.gov