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NCT01922518 Clinical Trial

Impact of Right Ventricular Pacing Determined by Electrocardiography

Atrioventricular Block Clinical Trial

— RVpacing  

Official title:
Impact of Right Ventricular Pacing Determined by Electrocardiography; Prospective Randomized Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01922518
Other study ID # SeoulStMary-RVP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2013
Est. completion date June 2019

Study information
Verified date April 2024
Source Seoul St. Mary's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Typically pacemaker electrode has been attached to the right ventricular apex. This method lead to Non-physiological Ventricular contraction. It has been reported to cause by ventricular dysfunction. In conclusion, this study demonstrate that impact of right ventricular pacing determined by electrocardiography was planned.

Description:

Patients who has Atrioventricular block scheduled for artificial pacemaker Randomized select 1:1 apex beats and ventricular septal beat.

Recruitment information / eligibility
Status Completed
Enrollment 233
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Atrioventricular block, pacemaker scheduled Exclusion Criteria: - History of myocardial infarction - Valvular heart disease (grade = 2 ) - History of Left ventricular dysfunction ( ejection fraction <50% or LV dimension >60 mm in the pre-procedure echocardiogram)

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Septal pacing
Put RV pacing lead around the right ventricular septum and is adjusted with normal pacing axis
• Apex pacing
Put RV lead around the apex

Locations
Country Name City State
Korea, Republic of Seoul st. mary's hospital Seoul Seo Cho Gu

Sponsors (1)
Lead Sponsor Collaborator
Yong Seog Oh

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary > 10% decrease of ejection fraction 3 years
See also
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