Percutaneous Left Atrial Appendage Occlusion
DevicePercutaneous left atrial appendage occlusion in routine care for patients with atrial fibrillation
NCT Number: NCT03279406
The objective of this observational non-randomized multicenter study is to compile real-world clinical characteristics and outcomes data for patients treated with LAA (left atrial appendage) closure systems in a daily clinical setting.
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Notify Me18 year–100 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Percutaneous left atrial appendage occlusion in routine care for patients with atrial fibrillation
Time frame: From date of inclusion until the date of first documented event, whichever came first, assessed up to 60 months
Death, Ischemic stroke, Transient ischemic attack, Major hemorrhage, Thrombus on device
University Hospital, Tours
Other
REgistry on Real-Life EXperience With Left Atrial Appendage Occlusion for Patients With Atrial Fibrillation in France
Acronym: RELEXAO
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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