Actively Recruiting
Evaluation of PWI Assisted by Marshall Ethanolization in Ablation of Persistent Atrial Fibrillation
Led by Xinhua Hospital, Shanghai Jiao Tong University School of Medicine · Updated on 2024-04-12
260
Participants Needed
1
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, randomized controlled, single-blind, multi-center clinical trial study aiming to investigate whether the strategy of posterior wall isolation (PWI) assisted by vein of Marshall ethanol infusion (VOMEI) could improve the success rate of persistent atrial fibrillation ablation.
CONDITIONS
Official Title
Evaluation of PWI Assisted by Marshall Ethanolization in Ablation of Persistent Atrial Fibrillation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between 18 and 85 years old
- Symptomatic, non-valvular persistent atrial fibrillation lasting at least 1 week
- Refractory to at least one antiarrhythmic drug
- Prepared to undergo atrial fibrillation catheter ablation
- Provide informed consent and agree to follow-up evaluations
You will not qualify if you...
- Acute myocardial infarction within the last 3 months
- Acute heart failure or new cerebral infarction within 3 months
- On the heart transplant list
- Life expectancy less than 1 year
- Untreatable bleeding disorders
- Presence of left atrial thrombus
- Heart failure with NYHA class III-IV or ejection fraction below 40%
- Uncontrolled malignant tumor
- Significant liver or kidney dysfunction (ALT, AST more than twice normal or creatinine clearance below 50%)
- Previous catheter ablation or cardiac surgery for atrial fibrillation
- Women who are pregnant, breastfeeding, planning pregnancy, or of childbearing age not using reliable contraception
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Xinhua Hospital, Shanghai Jiao Tong University
Shanghai, Shanghai Municipality, China, 200092
Actively Recruiting
Research Team
Y
Yichi YU, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here