Follow-up study in patients with re-implanted devices after transvenous lead extraction

Follow-up study in patients with re-implanted devices after transvenous lead extraction - Follow-up study in patients with re-implanted devices after transvenous lead extraction

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000049669

Enrollment

162

Registered

2022-12-02

Start date

2022-11-28

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients undergoing transvenous lead extraction(TLE) for implantable cardiac device infection or other reasons

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. TLE and reimplantation of the device 2. at least one device follow-up after device implantation and discharge from the hospital

Exclusion criteria

Exclusion criteria: 1. If the reimplanted device is an S-ICD (subcutaneous implantable cardioverter defibrillator) 2. When device follow-up has not been performed

Design outcomes

Primary

Measure	Time frame
Device follow-up data for patients with device reimplanted after TLE between 2016 and 2022	—

Countries

Japan

Contacts

Public ContactTsuyoshi Isawa

Sendai Kousei Hospital Department of cardiology

isa_tsuyo@yahoo.co.jp022-222-6181

Outcome results