Actively Recruiting
Left Atrial Appendage Closure Registry of Henri Mondor Hospital
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-01-15
250
Participants Needed
1
Research Sites
207 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Intro: Patients with atrial fibrillation are at significant risk of thrombus formation in the left atrial appendage, which can lead to strokes or systemic embolisms. This risk justifies first-line prescribing of long-term oral anticoagulant therapy in these patients. Percutaneous left atrial appendage closure, is an interventional cardiology technique for patients at high risk of stroke related to atrial fibrillation in whom long term anticoagulation therapy cannot be conducted. This procedure involves implantation of an occlusion device into the left atrial appendage to close it and prevent migration of thrombotic material that could otherwise cause distant embolism. Closure of the left atrial appendage avoids long-term prescription of anticoagulants while protecting patients against the risk of systemic embolism and stroke. Hypothesis/Objective: the main objective of this study is to assess the long term efficacy of left atrial closure, 5 years after the procedure Method: 150 patients will be included prospectively. We will also include restropectively100 other patients, previously treated by left atrial appendage closure at Henri Mondor hospital. Demographic, clinical, echocardiographic, and computed tomography data will be obtained by physical examination or medical records. Conclusion: this study will allow to assess the long term efficacy of left atrial closure in atrial fibrillation patients.
CONDITIONS
Official Title
Left Atrial Appendage Closure Registry of Henri Mondor Hospital
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Any patient for whom an indication has been made for implantation of a device for the closure of the left atrial appendage without restriction of indication and regardless of the outcome of the procedure (implantation success or not)
You will not qualify if you...
- Refusal of the patient to participate in this study
- Minor patient
- Patient not affiliated to the French social security system
AI-Screening
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Trial Site Locations
Total: 1 location
1
Assistance Publique Hôpitaux de Paris - CHU HENRI MONDOR
Créteil, France, 94010
Actively Recruiting
Research Team
E
Emmanuel Teiger, MD, PhD
CONTACT
P
Philippe Le Corvoisier, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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