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Active (not recruiting) Not applicable NCT05478304

Left Atrial Appendage Exclusion for Prophylactic Stroke Reduction Trial

No applicable phase (e.g. observational)
Conditions: Ischemic Stroke Systemic Embolism

Sponsor: AtriCure, Inc.

trial.available_in: БГ
Overview
This trial is a prospective, randomized, multicenter, multinational, blinded, superiority trial. The objective of this trial is to evaluate the effectiveness of left atrial appendage exclusion (LAAE) for the prevention of ischemic stroke or systemic arterial embolism in subjects undergoing cardiac surgery who have risk factors for atrial fibrillation and ischemic stroke.
Who can participate
Inclusion Criteria: * Subjects ≥ 18 years of age * Documentation of any of the following clinical criteria: * CHA2DS2-VASc ≥ 4 with age ≥ 65 * CHA2DS2-VASc ≥ 4 with significant left atrium enlargement or elevated NT-proBNP * CHA2DS2-VASc = 3 with age ≥ 75 * CHA2DS2-VASc = 3 with significant left atrium enlargement or elevated NT-proBNP * CHA2DS2-VASc score = 2 with age ≥ 65 and significant left atrium enlargement or elevated NT-proBNP Exclusion Criteria: * Clinically significant atrial fibrillation or atrial flutter: * Anytime in the past and * Documented by an electrocardiographic recording and * Episode lasting 6 minutes or longer1\* * Prior procedure involving opening the pericardium or entering the pericardial space * Prior LAA occlusion, exclusion, or removal (surgical or percutaneous) * Planned cardiac surgical procedure using non-sternotomy approaches o Partial sternotomies will be allowed. * Patients whose planned procedure is a heart transplant or implantation of any ventricular assist devices * Active endocarditis * Active systemic infection at the time of cardiac surgery requiring antibiotics, including known SARS-CoV2 infections regardless of symptoms * Known allergy to Nitinol or nickel sensitivity * Known medical condition with expected survival of less than 1 year * Other comorbidities that in the investigator's opinion make the subject unsuitable candidate to complete the protocol required visits. * Current enrollment in an investigation or trial or an investigational devices or investigational drug that would interfere with this trial. * Mental impairment or other psychiatric conditions which may not allow the patient to understand the nature, significance, and scope of the trial. * Pregnancy * Known severe symptomatic carotid disease
Locations 9
Australia (1)
Gold Coast University Hospital
Southport , Queensland
Belgium (1)
University Hospitals UZ Leuven
Leuven , Brabant
Canada (1)
Foothills Medical Centre
Calgary , Alberta
Czech Republic (1)
CKTCH Brno
Brno
Germany (1)
University Heart Venter Freiburg Bad Krozingen
Freiburg im Breisgau , Baden-Wurttemberg
New Zealand (1)
Waikato Hospital-Hamilton
Hamilton , Waikato Region
Spain (1)
Hospital Clinic Barcelona
Barcelona
United Kingdom (1)
Northern General Hospital
Sheffield , Great Britain
United States (1)
Heart Center Research / Huntsville Hospital
Huntsville , Alabama
Technical details
Status
Active (not recruiting)
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
25.01.2023
Completion date
01.04.2032
Registry ID
NCT05478304
Source
anzctr
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