MiniImal Defibrillation Threshold in With a Subcutaneous Implantable-Defibrillator Patients Undergoing Elective Generator Replacement.

Phase 2

Recruiting

• Conditions: Abnormal heart rhythm; ventricular arrhythmias; 10007521

• Registration Number: NL-OMON48785
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 45

Inclusion Criteria

Patients can be included if they:
- are over 18
- are able to give informed consent
- will undergo S-ICD generator replacement and subsequent defibrillation
threshold testing (DFT)

Exclusion Criteria

Patients who will not undergo defibrillation testing as part of their regular
care due toa contra-indication.
Patients with a BMI < 18.5 kg/m2

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Outcome<br /><br>The main outcome will be the lowest energy on which defibrillation of the<br /><br>induced ventricular arrhythmia was successful after replacement of the S-ICD<br /><br>generator.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable. </p><br>