Clinical Trials Directory

Trials / Completed

CompletedNCT00180323

ACC - Atrial Contribution to CRT

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Boston Scientific Corporation · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This prospective study will evaluate in patients, fulfilling implant criteria for Cardiac Resynchronisation Therapy (CRT) implant, the optimal atrial contribution to the resynchronised ventricles in the event of right atrial pacing.

Detailed description

All patients will undergo advanced echocardiographic examination pre-operative, pre-discharge after implantation and at 3 and 6-months follow-up. AV-delay optimization will be performed using aortic VTI measured by continuous wave Doppler in a modified 4-chamber view. During optimisation aortic VTI will be measured at different heart rates reached by increasing atrial pacing 10, 20 and 30 beats above intrinsic heart rate (IHR).

Conditions

Interventions

TypeNameDescription
DEVICERenewalRenewal is a CRT-D device for cardiac resynchronization therapy

Timeline

Start date
2004-11-01
Primary completion
2008-12-01
Completion
2008-12-01
First posted
2005-09-16
Last updated
2021-02-11
Results posted
2012-11-12

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00180323. Inclusion in this directory is not an endorsement.

ACC - Atrial Contribution to CRT (NCT00180323) · Clinical Trials Directory