Skip to main content
Clinical Trials/NCT00508196
NCT00508196
Completed
Not Applicable

Endothelial Function and Cardiac Output in Right Ventricular Pacing

University of Dundee1 site in 1 country22 target enrollmentNovember 2006
ConditionsBradycardia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bradycardia
Sponsor
University of Dundee
Enrollment
22
Locations
1
Primary Endpoint
Endothelial Function Assessed by Flow Mediated Vasodilatation
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Pacing from the right ventricle (as is current practice in patients implanted with permanent pacemakers for bradycardia), has been associated with worse outcomes particularly in heart failure patients. Recent clinical trials suggest that chronic right ventricular pacing (VP) is associated with worsening heart failure, increased strokes and atrial fibrillation. Hemodynamically, right VP results in delayed activation and contraction of the LV which can give rise to functional mitral regurgitation, shortened diastolic filling time and thus reduced coronary filling, as well as abnormal arterial pulsatile flow. The mechanisms for the deleterious effects of right VP in heart failure patients have not been previously investigated. Our aim of this study is therefore to investigate the hemodynamic effects of right VP in stable heart failure patients in terms of exercise cardiac output (CO, an important measure of myocardial function and prognosis), as well as endothelial function which may be deranged as a result of abnormal arterial pulsatile flow.

Detailed Description

Study Aims The aim of this study is to investigate the effect of right ventricular pacing on CO at rest and exercise, and on endothelial function and B-type natriuretic peptide, BNP, in patients with heart failure. Methods: Thirty patients with dual chamber pacemakers for sinus node disease will be recruited: 15 controls with normal LV function and 15 with stable impaired LV function (ejection fraction \<40%). The pacemaker will be programmed to pace to back-up pacing at 55bpm in the atrial only (AAI, no right VP) for one week (baseline); and than programmed to overdrive pacing at 70-80bpm, randomised to either to dual chamber, DDD (sequential atrial and ventricular pacing) with a short AV delay (to ensure maximal right VP) or AAI (no RV pacing), for 1 week. There will be a crossover after a 1 week washout at backup AAI pacing at 55 bpm. Resting and exercise CO will be measured at the end of each pacing mode intervention using the Inocor system (a validated non invasive method of CO measurement, using inhaled inert gas equilibriums). Endothelial function will be measured non-invasively at the same time points, as will plasma BNP, a measure of LV strain. Patients with unstable heart failure or angina will be excluded. Study Endpoints: Rest and exercise CO; and endothelial function and BNP with and without RV pacing, in patients with preserved and impaired LV function.

Registry
clinicaltrials.gov
Start Date
November 2006
End Date
July 2007
Last Updated
7 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Dual chamber pacemaker
  • Intact AV node function

Exclusion Criteria

  • Unstable angina, heart failure
  • Inability to exercise

Outcomes

Primary Outcomes

Endothelial Function Assessed by Flow Mediated Vasodilatation

Time Frame: 1 week

Flow mediated vasodilatation as measured by reactive hyperaemia peripheral arterial tonometry signal using EndoPAT software, Itamar. A post-occlusion to pre-occlusion ratio is calculated by the EndoPAT software, providing the EndoPAT index (EnFI)

Secondary Outcomes

  • Cardiac Output(1 week)
  • B-type Natriuretic Pepetide(1 week)

Study Sites (1)

Loading locations...

Similar Trials