Assessing frailty in patients undergoing left atrial appendage closure
Official title: Frailty in Patient Undergoing Percutaneous Left Atrial Appendage Closure The Frail-LAAC Study
Run by Institut universitaire de cardiologie et de pneumologie de Québec, University Laval · NCT05257954 · Data updated 2026-11-12
This study is trying to see how frailty affects the health and quality of life of patients getting a specific heart procedure called left atrial appendage closure.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Institut universitaire de cardiologie et de pneumologie de Québec, University Laval Academic / other |
| Locations | 1 site (Québec, Quebec) |
| Status | Recruiting |
| Started | March 1, 2022 |
| Main results expected | March 1, 2027 |
| Study ends | March 1, 2029 |
| Registry record updated | March 24, 2026 |
| Trial ID | NCT05257954 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 and older who are undergoing transcatheter LAAC.
✕Probably not a fit
Patients who are unable to provide informed consent or have severe neuropsychiatric impairment may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to evaluate the prevalence and severity of frailty in patients who are undergoing transcatheter left atrial appendage closure (LAAC). It will investigate the relationship between frailty and both peri-procedural and long-term outcomes, as well as the impact on patients' quality of life. The study recognizes that while LAAC is a promising alternative to anticoagulation therapy, the high-risk nature of the patient population necessitates better selection criteria to improve outcomes. By understanding frailty in this context, the study seeks to enhance patient management and procedural success.
Why it matters
Potential benefit: If successful, this study could lead to improved patient selection and outcomes for those undergoing LAAC.
How similar studies have gone: Other studies have highlighted the importance of patient selection in LAAC procedures, indicating that this approach is relevant and necessary.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Transcatheter LAAC with any approved device * Age ≥18 years old Exclusion Criteria: * Unable to provide informed consent * Severe neuropsychiatric impairment
Where it's running
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Iucpq_ul
Québec, Quebec, Canada Recruiting
Study contacts
- Study coordinator: Josep Rodes-Cabau, MD, PhD
- Email: josep.rodes@criucpq.ulaval.ca
- Phone: 418-656-8711
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.