CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 178 enrolled
Drug / intervention
CRT-D and LV lead (Quartet™ lead and Promote Q® device system)device
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/NCT00990665
NCT00990665N/ACompleted

Promote Q CRT-D and Quartet Left Ventricular Heart Lead Study

Abbott Medical Devices·interventional·Posted Oct 7, 2009·Updated Feb 27, 2019

In Brief

A clinical study evaluating CRT-D and LV lead (Quartet™ lead and Promote Q® device system) for Heart Failure. Completed, enrolled 178 participants across 24 sites.

Detailed Summary

The objective of this study is to assess the safety and efficacy of the Quartet™ lead and Promote Q® device system in a patient population indicated for cardiac resynchronization therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHeart Failure
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 7, 2009
Enrollment StartSep 1, 2009
Primary CompletionSep 1, 2010
Study CompletionJul 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 16.7 years ago

Interventions

CRT-D and LV lead (Quartet™ lead and Promote Q® device system)device

Promote Q CRT-D and Quartet LV lead