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NCT Number: NCT07403760

Wellbeing and Survival Improvement With Event Reduction by Ablation for Atrial Fibrillation in the Very Elderly

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.

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Key information

Age range

80 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beijing Anzhen Hospital, Capital Medical University, Beijing, China

Beijing, China

Location status: Recruiting

Location contact

Changsheng Ma, Prof.

PRINCIPAL_INVESTIGATOR

Liu He, PhD.

CONTACT

[email protected]

+86 13810720787

Ning Zhou, Prof.

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 80 years.
  • Documented paroxysmal or persistent atrial fibrillation by ECG or Holter within 6 months prior to enrollment.
  • Symptomatic AF (including palpitations, chest tightness, fatigue, dizziness, blackouts, dyspnea).
  • Voluntary participation and signed informed consent.

Exclusion criteria

  • NYHA Class IV heart failure.
  • Acute myocardial infarction, cardiac surgery, or PCI within the past 1 year.
  • Long-standing persistent AF (duration > 1 year).
  • Left atrial anteroposterior diameter > 6 cm.
  • History of prior AF ablation.
  • AF secondary to reversible causes (e.g., post-surgery, infection, hyperthyroidism).
  • Severe mitral stenosis.
  • Moderate to severe hepatic failure (Child-Pugh B-C).
  • Renal failure stage 4-5 (eGFR <30 ml/min/1.73m2) or continuous dialysis.
  • Inability to cooperate due to dementia or severe mental disorder.
  • Presence of left atrial thrombus.
  • Prior Left Atrial Appendage Occlusion (LAAO).
  • Contraindication to anticoagulation.
  • Life expectancy < 1 year.

Treatment and study plan

Catheter ablation

Procedure

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.

Sham Control

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).

Primary outcomes

  1. Change in SF-36 Total Score

    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.

Secondary outcomes

  1. Change in AFEQT Score

    Time frame: Baseline, 6 months

    Change in Atrial Fibrillation Effect on Quality-of-Life (AFEQT) score

  2. Change in Clinical Frailty Scale (CFS) Score

    Time frame: Baseline, 6 months

    Change in frailty status assessed by CFS

  3. Change in Left Ventricular Ejection Fraction (LVEF)

    Time frame: Baseline, 6 months

  4. Change in NT-proBNP level

    Time frame: Baseline, 6 months

  5. Freedom from Atrial Arrhythmias

    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.

  6. Incidence of Composite Cardiovascular Outcome

    Time frame: 6 months

    Composite of all-cause death, stroke or systemic embolism, myocardial infarction, major bleeding, and heart failure hospitalization/emergency visits.

  7. Healthcare Resource Utilization

    Time frame: 6 months

    Number of emergency room visits and unplanned hospitalizations

Other outcomes

  1. Safety Outcome

    Time frame: 6 months

    Composite of all-cause death, stroke, serious adverse events and complications

Study contacts

Contact information is provided by the study sponsor or research team.

Liu He, PhD

CONTACT

[email protected]

+86 13810720787

Sponsors and collaborators

Lead sponsor

Beijing Anzhen Hospital

Other

Registry information

Official study title

Wellbeing and Survival Improvement With Event Reduction by Ablation for Atrial Fibrillation in the Very Elderly (WISER-AF)

Acronym: WISER-AF

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Feb 11, 2026
Registry last updated
Jul 6, 2026

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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