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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02485093
Other study ID # 2008-A01266-49
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2009
Est. completion date October 2014

Study information

Verified date February 2019
Source Abbott Medical Devices
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Optimal pacing strategy for patients with SND is still unknown, although several publications in the past years demonstrated a deleterious effect of ventricular pacing. However, pacing has always been apical in these trials, and to which extent this absence of pacing is beneficial for patients with very long PR intervals is still to be found.

The aim of this study is to compare ventricular septal pacing to no pacing in patients with SND.


Recruitment information / eligibility

Status Completed
Enrollment 215
Est. completion date October 2014
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with sinus node disease

Exclusion Criteria:

- Complete or high degree AV block

- Permanent atrial fibrillation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Septal ventricular pacing
Ventricular pacing must be at least 90%, from the septum and with optimized AV delay
VIP
Ventricular pacing must be less than 10%.

Locations

Country Name City State
France CHU Pontchaillou - CCP Rennes

Sponsors (1)

Lead Sponsor Collaborator
Abbott Medical Devices

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Left Ventricular Endsystolic Diameter (LVED) 18 months
Secondary AF incidence 18 months
Secondary Hospitalizations 18 months
See also
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