Follow-up study in patients with re-implanted devices after transvenous lead extractio
Not Applicable
- Conditions
- Patients undergoing transvenous lead extraction(TLE) for implantable cardiac device infection or other reasons
- Registration Number
- JPRN-UMIN000049669
- Lead Sponsor
- Sendai Kousei Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 162
Inclusion Criteria
Not provided
Exclusion Criteria
1. If the reimplanted device is an S-ICD (subcutaneous implantable cardioverter defibrillator) 2. When device follow-up has not been performed
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Device follow-up data for patients with device reimplanted after TLE between 2016 and 2022
- Secondary Outcome Measures
Name Time Method