CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 83 enrolled
Drug / intervention
Bi-ventricular Implantable Cardioverter Defibrillatordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00526162
NCT00526162N/ACompleted
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Clinical Study to Evaluate System Safety and Clinical Performance of the ConsultaTM CRT-D Device

Medtronic Cardiac Rhythm and Heart Failure·interventional·Posted Sep 10, 2007·Updated Jul 2, 2025

In Brief

A clinical study evaluating Bi-ventricular Implantable Cardioverter Defibrillator for Tachyarrhythmias and 2 related conditions. Completed, enrolled 83 participants across 1 site.

Detailed Summary

The purpose of the Consulta clinical study is to evaluate the overall system safety and clinical performance of the Consulta Implantable Cardioverter Defibrillator with Cardiac Resynchronization Therapy (CRT-D).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTachyarrhythmias, Heart Failure, Ventricular Dysfunction
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 10, 2007
Enrollment StartOct 1, 2007
Primary CompletionJan 1, 2008
Study CompletionOct 1, 2008
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 18.8 years ago

Interventions

Bi-ventricular Implantable Cardioverter Defibrillatordevice

Implantation of a Bi-ventricular Implantable Cardioverter Defibrillator