Flexible Transseptal Puncturewire

Completed

• Conditions: nvt; 10007521

• Registration Number: NL-OMON33579
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 10

Inclusion Criteria

All patients that have to undergo a transseptal puncture for catheter ablation of atrial fibrillation or of an accessory left sided atrio-ventricular connection.

Exclusion Criteria

Patients who have undergone an earlier transseptal puncture.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Success of the transseptal puncture (yes/no), duration of this part of the<br /><br>procedure, and possible complications.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Technical issues that may have to be improved.</p><br>