ECG Monitoring Short vs Middle Term After Atrial Fibrillation Ablation
Active, not recruiting
- Conditions
- Atrial Fibrillation
- Registration Number
- NCT05959915
- Lead Sponsor
- Hospital Clinic of Barcelona
- Brief Summary
To compare the number of patients with AF recurrence detected in a 24-h Holter monitoring with a 5-day record.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
- Have undergone an AF ablation procedure at the Hospital Clínic and have a 12-month follow-up planned.
- Having been previously assessed by the AF nurse.
- Having signed the informed consent.
Exclusion Criteria
- Extreme skin fragility at chest level
- Allergy to latex or adhesive tape
- No electrophysiology follow-up at the Clínic hospital.
- Patients who are already included in other studies that may interfere with the expected results of this one.
- Patients with cognitive impairment or disorientation.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method AF recurrence up to 5 days Number of patients with AF recurrence detected in a cardio loop monitoring.
- Secondary Outcome Measures
Name Time Method Total time of noise up to 5 days Total time of noise in each group
time to analyze min:hours time it takes to analyze and interpret the logs obtained, in minutes.
Adverse effects up to 5 days skin injuries, losses, allergies, etc.
Burden of AF up to 5 days Burden of AF in the two groups (Day/Hours/minuts)
Number of patients with recurrent AF / atrial flutter / atrial tachycardia up to 5 days Number of patients with recurrent AF / atrial flutter / atrial tachycardia in two groups
Total time analized up to 5 days Total time analized in each group
premature losses up to 5 days loss of connection of the device before 5 days
Trial Locations
- Locations (1)
Hospital Clínic Barcelona
🇪🇸Barcelona, Spain