The Single-center Prospective Randomized Controlled Trial Evaluating Efficacy and Safety of Catheter Ablation without Periprocedual Contrast Media for Paroxysmal Atrial Fibrillation: Sophisticated Atrial Fibrillation ablation procedurE contrasT media unnecessitY (SAFETY) trial
Not Applicable
- Conditions
- Paroxysmal atrial fibrillation
- Registration Number
- JPRN-UMIN000023100
- Lead Sponsor
- Kyoto University Graduate School of Medicine,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients with a history of allergy for contrast media 2)Patients with renal insufficiency (eGFR <=45ml/min/1.73m2 3)Left ventricular ejection fraction < 40% 4)Left atrial diameter > 50mm 5)Patients with a history of open heart surgery 6)Patients with moderate or severe valve heart disease 7)Patients who need additional ablation such as tricuspid valve isthmus ablation during procedure 8)Patients unwilling to sign the consent form for participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method