Dual site versus single site irrigated tip catheters in the ablation of atrial flutter

Completed

• Conditions: Atrial flutter; Circulatory System; Atrial fibrillation and flutter

• Registration Number: ISRCTN45640987
• Lead Sponsor: Oxford Radcliffe Hospitals NHS Trust (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-04-20
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 63

Inclusion Criteria

1. Patient/subject or legal representative is willing and able to give informed consent for participation in the study
2. Male or female, aged 18 years or above
3. Diagnosed with atrial flutter

Exclusion Criteria

Pregnancy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Radiofrequency time to cavotricuspid isthmus block, time from when ablation starts to when the procedure is deemed complete.

Secondary Outcome Measures

Name	Time	Method
1. Fluoroscopy time to cavotricuspid isthmus block, the amount of x-ray screening time needed for the primary endpoint to be achieved<br>2. Total procedure time, includes all time, i.e., not only the primary endpoint time but any additional time of the procedure before and after