Comparison of the Safety and Efficacy of the Management of Pacemaker Patients Followed-up via Home Monitoring vs. Conventional In-office Follow-ups
Not Applicable
- Conditions
- Arrhythmia
- Registration Number
- JPRN-UMIN000007377
- Lead Sponsor
- Biotronik Japan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 1364
Inclusion Criteria
Not provided
Exclusion Criteria
*Contraindicated for IPG under Japanese guidelines *Patients who are currently included in another cardiac clinical study *Patients with expected life period of less than 27 months *Patients who might undergo heart transplantation in next 27 months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method