Beijing Anzhen Hospital, Capital Medical University, Beijing, China
Beijing, China
Location status: Recruiting
Location contact
Changsheng Ma, Prof.
PRINCIPAL_INVESTIGATOR
Liu He, PhD.
CONTACT
Ning Zhou, Prof.
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07403760
The WISER-AF trial is a multicenter, double-blind, sham-controlled, randomized controlled trial. It aims to evaluate the efficacy and safety of catheter ablation compared to a sham procedure in improving the quality of life (SF-36 score) in very elderly patients (aged ≥80 years) with symptomatic atrial fibrillation over a 6-month follow-up period.
Interested in participating?
Request Info80 year and older
All sexes
Interventional
Not applicable
Beijing, China
Location status: Recruiting
Changsheng Ma, Prof.
PRINCIPAL_INVESTIGATOR
Liu He, PhD.
CONTACT
Ning Zhou, Prof.
PRINCIPAL_INVESTIGATOR
Atrial fibrillation (AF) prevalence increases with age, posing significant challenges in the very elderly (≥80 years). While catheter ablation is an established treatment for general AF patients, its efficacy in improving quality of life (QoL) in the very elderly remains underrepresented in previous trials. The WISER-AF trial is designed to fill this evidence gap. The study will enroll 136 symptomatic AF patients aged ≥80 years in China. Patients will be randomized 1:1 to undergo either catheter ablation or a sham procedure. To ensure blinding, all patients will wear eye masks and headphones during the procedure. The sham group will receive phrenic nerve stimulation to mimic the sensation of ablation without delivering therapeutic energy. The primary endpoint is the change in the SF-36 total score from baseline to 6 months. Secondary endpoints include changes in AFEQT score, Clinical Frailty Scale (CFS), LVEF, NT-proBNP, and cardiovascular events.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients undergo PVI (for paroxysmal AF) or PVI +linear ablation+EI-VOM(for persistent AF). All patients will wear eye masks and headphones with music during the procedure.
Patients undergo femoral vein puncture and catheter placement. Phrenic nerve stimulation is performed to mimic procedural sensations. No ablation energy is delivered. All patients will wear eye masks and headphones with music during the procedure. Patients remain in the lab for at least 60 minutes (for paroxysmal AF) or 90 minutes (for persistent AF).
Time frame: Baseline, 6 months
Difference in the change of the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36) total score from baseline to 6 months between the two groups.
Time frame: Baseline, 6 months
Change in Atrial Fibrillation Effect on Quality-of-Life (AFEQT) score
Time frame: Baseline, 6 months
Change in frailty status assessed by CFS
Time frame: Baseline, 6 months
Time frame: Baseline, 6 months
Time frame: 6 months
Absence of atrial fibrillation, atrial flutter, or atrial tachycardia recorded by ECG, Holter, or patch monitor after a 30-day blanking period.
Time frame: 6 months
Composite of all-cause death, stroke or systemic embolism, myocardial infarction, major bleeding, and heart failure hospitalization/emergency visits.
Time frame: 6 months
Number of emergency room visits and unplanned hospitalizations
Time frame: 6 months
Composite of all-cause death, stroke, serious adverse events and complications
Contact information is provided by the study sponsor or research team.
Beijing Anzhen Hospital
Other
Wellbeing and Survival Improvement With Event Reduction by Ablation for Atrial Fibrillation in the Very Elderly (WISER-AF)
Acronym: WISER-AF
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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