Actively Recruiting
Comparison of 3 RF Delivery Modes of the QDOT Catheter for Paroxymal Atrial Fibrillation (AF) Ablation
Led by Institut Mutualiste Montsouris · Updated on 2024-10-17
90
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Pulmonary vein isolation is the main treatment of paroxysmal and persistent atrial fibrillation. The aim of our study is to prospectively compare the efficacy and safety of the 3 options of radiofrequency delivery with QDOT Micro™, with systematic use of catheter stabilization tools and tighter lesions
CONDITIONS
Official Title
Comparison of 3 RF Delivery Modes of the QDOT Catheter for Paroxymal Atrial Fibrillation (AF) Ablation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 18 or over
- First atrial fibrillation ablation
- Paroxysmal atrial fibrillation lasting less than 48 hours
- Early atrial fibrillation lasting between 7 days and 3 months
- At least one episode of atrial fibrillation in the year before joining the study
- Patient affiliated to a health insurance
You will not qualify if you...
- History of atrial fibrillation ablation (surgery or catheter)
- Documented left atrial thrombus
- Left atrial diameter greater than 60mm, area greater than 35cm2, or volume index greater than 45ml/m2
- Heart attack, angioplasty, or valve replacement within 3 months before joining
- Any contraindication to the use of the QDOT MICRO12 bidirectional navigation catheter
- Patient unable to understand study information
- Patient deprived of liberty by judicial or administrative decision
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Institut Mutualiste Montsouris
Paris, Paris, France, 75014
Actively Recruiting
Research Team
N
Naly ANDRIAMBAO
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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