Inappropriate implantable cardioverter-defibrillator therapy: Frequency, syncope and prognostic factors

Inappropriate implantable cardioverter-defibrillator therapy: Frequency, syncope and prognostic factors - Inappropriate ICD therapy survey

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000025995

Enrollment

200

Registered

2017-02-04

Start date

2014-10-30

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

Life-threatening arrhythmia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: To be enrolled, patients had to: (1) have an indication for ICD or CRT-D implantation according to the JCS Guidelines for Device-based Therapy of Cardiac Rhythm Abnormalities (2) be able to visit scheduled outpatient department and (3) be able to comply with the study protocol.

Exclusion criteria

Exclusion criteria: Patient exclusion criteria were no information on the medical condition, refused enrollment of this study.

Design outcomes

Primary

Measure	Time frame
The incidence of syncope related to inappropriate ICD therapies.	—

Secondary

Measure	Time frame
The prognostic factors in patients who had inappropriate ICD therapies.	—

Countries

Japan

Contacts

Public ContactEiichi Watanabe

Fujita Health University School of Medicine Department of Cardiology

enwatan@fujita-hu.ac.jp0562-93-2312

Outcome results