Study of atrial fibrillation-burden and -pattern in patients with implanted device
- Conditions
- I48Atrial fibrillation and flutter
- Registration Number
- DRKS00027420
- Lead Sponsor
- niversitätsklinikum Essen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
1) Patients with a BIOTRONIK dual-chamber ICD, DX, CRT-D, CRT-P, or pacemaker
2) Inclusion no earlier than 4 weeks after implantation
3) Patients's agreement to use CardioMessenger® and BIOTRONIK Home Monitoring®
4) Age = 18 years
1st group: Documented paroxysmal or persistent atrial fibrillation and increased NT-pro-BNP (> 125pg / ml) within the last 8 weeks
2nd group: Sinus rhythm and CHA2DS2VASc value = 4 or sinus rhythm and increased NT-proBNP (> 125pg / ml) within the last 8 weeks
Exclusion Criteria
1. Life expectancy <1 year
2. Inability of the patient to complete the study protocol
3. Known alcohol or drug addiction
4. Participation in another interventional clinical study
5. Existing or currently planned pregnancy
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method