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
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