Respiratory monitoring and clinical outcome in patients with implantable cardioverter-defibrillator

Not Applicable

• Conditions: Heart failure

• Registration Number: JPRN-UMIN000026322
• Lead Sponsor: Department of Cardiology Fujita Health University School of Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2016-12-31
• Study Start: 2017-03-06
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Not provided

Exclusion Criteria

Inability or refusal to sign the Subject Informed Consent or inability of refusal to comply with the follow-up schedule Contraindication for ICD or CRT-D Have received or will receive heart transplant Receiving mechanical circulatory support A life expectancy of less than 12 months due to non-cardiac cause Documented as pacemaker dependent Pregnant or lactating Less than 18 years of age Enrolled in any other clinical study

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Acute exacerbation of heart failure

Secondary Outcome Measures

Name	Time	Method
To examine associations betwen changes in the biosignal including respiratory rate, sleep disordered bleething, heart rate, and patient activity and clinical characteristics or clinical outcomes