Pacemaker-based Long-term Monitoring of Sleep Apnea
Recruiting
Observational Study
Bradycardia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,000 (estimated)
- Sponsor
- Medical University Innsbruck · Other
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About This Trial
This is a prospective, non-interventional cohort study. It tests the hypothesis that
* Pacemaker-derived monitoring of sleep-related breathing disorders and/or daily physical activity predicts clinical outcome.
* Autonomic imbalance defined by an increased periodic repolarisation dynamics (PRD) predicts clinical outcome in pacemaker patients.
* Autonomic imbalance defined by an increased periodic…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* implanted Microport TEO SR/DR or BOREA SR/DR or ALIZEA SR/DR pacemaker device
* signed informed consent
Exclusion Criteria:
* any contraindication to perform a cardiac CT examination
* eGFR \< 30 ml/min/1.73 m2
* allergy against CT contrast medium
* hyperthyreoism
* inabilit…
Contacts
No contact information available.