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Clinical Trials/NCT00709384
NCT00709384
Completed
Phase 2

Prevention of Atrial Tachycardia After a Right Atriotomy II

Aarhus University Hospital Skejby1 site in 1 country14 target enrollmentJanuary 2006
ConditionsAtrial Flutter

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Atrial Flutter
Sponsor
Aarhus University Hospital Skejby
Enrollment
14
Locations
1
Primary Endpoint
completeness of the lines of block
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The investigators performed a prophylactic peroperative linear lesions connecting the tricuspid annulus with a right atriotomy and the atriotomy with the inferior caval vein to prevent atrial flutter on 15 consecutive adult patients undergoing surgery for congenital heart disease. Conduction time between electrodes placed on both sides of the lesions is measured on the second postoperative day. Coronary angiography and electrophysiology study using an electroanatomic mapping system to assess conduction across the line are performed three month after the operation.

Detailed Description

We perform a prophylactic peroperative linear lesions connecting the tricuspid annulus with a right atriotomy (surgical dissection plus cryoablation) and the atriotomy with the inferior caval vein (cryoablation alone) to prevent atrial flutter on 15 consecutive adult patients undergoing surgery for congenital heart disease. Conduction times between electrodes placed on both sides of the lesions are measured on the second postoperative day. Coronary angiography and electrophysiology study using an electroanatomic mapping system to assess conduction across the line and to try to induce atrial flutter are performed three month after the operation.

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
March 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Aarhus University Hospital Skejby

Eligibility Criteria

Inclusion Criteria

  • Clinical indication for corrective operation for congenital heart disease with the use of a right lateral atriotomy,
  • Age \>18 years,
  • Ability to give an informed consent.

Exclusion Criteria

  • Acute operation
  • Chronic atrial fibrillation
  • Indication for MAZE procedure

Outcomes

Primary Outcomes

completeness of the lines of block

Time Frame: 3 month

Secondary Outcomes

  • safety(3 month)

Study Sites (1)

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