PRospEctive multiCenter registry to InveStigate the clinical fEasibility of COMBination wOrkflow with 90W/4sec and Ablation index-guided 50W ablation (PRECISE-COMBO 90W/50W study)
Not Applicable
Recruiting
- Conditions
- Atrial fibrillation
- Registration Number
- JPRN-UMIN000050344
- Lead Sponsor
- Division of Cardiology, Department of Medicine, Nihon University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with persistent atrial fibrillation. 2) Patients with a history of ablation 3) Patients who have difficulty in taking oral medication 4) Patients on dialysis 5) Patients with severe valvular heart disease 6) Patients who have difficulty in obtaining consent in person 7) Patients who have refused to participate in this study. 8) Any other Patients who are judged by the principal investigator to be unsuitable as a research subjects.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method success rate of first-pass pulmonary vein isolation
- Secondary Outcome Measures
Name Time Method