Clinical Trials Directory

Trials / Terminated

TerminatedNCT01475175

Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exercise (AdOPT CRT)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Medtronic Cardiac Rhythm and Heart Failure · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The AdOPT Cardiac Resynchronization Therapy (CRT) study is an acute, prospective, multi-center, non-randomized investigational study designed to compare indices of cardiac function at device settings optimized using the investigational Adaptive CRT (aCRT) algorithm versus nominal programming. The comparison will be performed during rest, atrial pacing and sub-maximal exercise. AdOPT CRT is a sub study of the Adaptive CRT Study (NTC00980057) being conducted in Europe.

Detailed description

Adaptive CRT is an implantable heart failure device feature that attempts to optimize CRT without echocardiographic testing.

Conditions

Interventions

TypeNameDescription
DEVICECRT pacing at rest and during exerciseCRT pacing with aCRT settings and BiV pacing with nominal programming at rest and during submaximal exercise

Timeline

Start date
2011-11-01
Primary completion
2012-03-01
Completion
2012-03-01
First posted
2011-11-21
Last updated
2019-08-05
Results posted
2012-10-12

Locations

7 sites across 6 countries: Austria, Belgium, Denmark, Germany, Netherlands, Norway

Source: ClinicalTrials.gov record NCT01475175. Inclusion in this directory is not an endorsement.