MedPath

STroke Secondary Prevention With Catheter ABLation and EDoxaban for Patients With Non-valvular Atrial Fibrillation: STABLED Study

Phase 3
Active, not recruiting
Conditions
Ischemic Stroke
Atrial Fibrillation Non-Rheumatic
Interventions
Procedure: Catheter ablation
Registration Number
NCT03777631
Lead Sponsor
Nippon Medical School
Brief Summary

Catheter ablation (CA) has been reported to reduce risk of stroke in patients with nonvalvular atrial fibrillation (NVAF) in retrospective studies, but risk and benefit of CA has not been well elucidated in NVAF with recent cerebral infarction in prospective randomized trials.

Detailed Description

In patients with NVAF, stroke is an independent risk factor for a subsequent cerebral infarction. Although anticoagulant therapy can effectively reduce thromboembolic events, the reported annual recurrence rate in NVAF and previous stroke patients in the "real-world" is not low even with appropriate antithrombotic treatment; 8.6% in patients with "guideline adherent" antithrombotic therapy and around 5% in patients treated with anticoagulant therapy. NVAF and recent stroke is high-risk population for stroke recurrence even with anticoagulant therapy, and developing optimal secondary prevention strategy is an urgent task.

Catheter ablation (CA) is now widely used to treat symptoms related to NVAF. Some retrospective studies showed a beneficial effect of CA for stroke prevention using age-/sex-matching or propensity-score matching. Moreover, CA have a potential to improve survival or prevent heart failure development in patients with AF. However, the effect of CA for secondary stroke prevention or impact of CA for NVAF patients with recent ischemic stroke for survival or developing heart failure has not been evaluated in a prospective randomized trial. Therefore, in the present study, we intend to compare two groups of patients with NVAF with a history of cerebral infarction: a group receiving standard medical therapy (control group) and a group receiving standard medical therapy plus CA (CA group).

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
251
Inclusion Criteria
  • Age ≥20 or ≤85 years at time of giving informed consent
  • Nonvalvular atrial fibrillation
  • History of stroke in previous 6 months
  • Current or planned treatment with edoxaban
  • Modified Rankin scale ≤3
Exclusion Criteria
  • Symptomatic paroxysmal AF resistant to anti-arrhythmic drugs
  • Presence of left atrial thrombus and left atrial appendage on transthoracic echocardiography, computed tomography or magnetic resonance imaging
  • Unable to take anticoagulation therapy for any reason, including tendency to bleed or considered at high risk for bleeding from anticoagulation therapy.
  • Presence of severe renal disorder (estimated creatinine clearance <30 mL/min by Cockroft-Gault equation)
  • Previous CA or surgical intervention for AF
  • History of treatment with a left atrial appendage closure device
  • Left atrial diameter ≥55 mm on transthoracic echocardiography
  • Ejection fraction ≤35% on transthoracic echocardiography
  • Persistent AF for ≥10 years
  • Pregnant or possibility of pregnancy
  • Unlikely to complete the study, such as due to progressive malignant tumor
  • Participating or planning to participate in another clinical trial
  • Unwilling to participates
  • Judged as incompatible for the study by the investigators

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Catheter ablation groupCatheter ablationCatheter ablation (CA) should be performed within 1-6 months from the onset of cerebral infarction. CA is based on pulmonary vein isolation, with atrial ablation as required. For conducting CA by a trained and experienced cardiologist, only institutions in which performed \>100 CA annually were participated in the present study in principle.
Primary Outcome Measures
NameTimeMethod
Composite of recurrence of cerebral infarction, systemic embolism, all-cause death, hospitalization for heart failure.Up to 6 years

Composite of recurrence of cerebral infarction, systemic embolism, all-cause death, hospitalization for heart failure.

Secondary Outcome Measures
NameTimeMethod
Recurrence of cerebral infarction in patients with or without discontinuation of EdoxabanUp to 6 years

Recurrence of cerebral infarction in patients with or without discontinuation of Edoxaban

Any bleedingUp to 6 years

Any bleeding

Hospitalization for heart failureUp to 6 years

Hospitalization for heart failure

Recurrence of cerebral infarctionUp to 6 years

Recurrence of cerebral infarction

All-cause deathUp to 6 years

All-cause death

Cardiovascular deathUp to 6 years

Cardiovascular death

Intracranial hemorrhageUp to 6 years

Intracranial hemorrhage

Composite eventsUp to 6 years

all-cause death, onset of stroke, systemic embolism, hospitalization for heart failure, and serious adverse event caused by CA

The rate of and related factors to discontinuation of EdoxabanUp to 6 years

The rate of and related factors to discontinuation of Edoxaban

Systemic embolismUp to 6 years

Symptomatic systemic embolism to other regions than brain, e.g. peripheral or visceral arteries

Trial Locations

Locations (46)

Nippon Medical School Chiba Hokusoh Hospital

🇯🇵

Chiba, Japan

Iwate Medical University

🇯🇵

Morioka, Japan

Nagasaki University Hospital

🇯🇵

Nagasaki, Japan

Saga Medical Center Koseikan

🇯🇵

Saga, Japan

New Tokyo Heart Clinic

🇯🇵

Chiba, Japan

Tsuruoka Kyoritsu Hospital

🇯🇵

Yamagata, Japan

Fukuyama Cardiovascular Hospital

🇯🇵

Hiroshima, Japan

Suiseikai Kajikawa Hospital

🇯🇵

Hiroshima, Japan

New Tokyo Hospital

🇯🇵

Chiba, Japan

Kokura Memorial Hospital

🇯🇵

Fukuoka, Japan

National Hospital Organization Kanazawa Medical Center

🇯🇵

Kanazawa, Japan

Saiseikai Kumamoto Hospital

🇯🇵

Kumamoto, Japan

Tokyo Women's Medical University Hospital

🇯🇵

Tokyo, Japan

Ichinomiyanishi Hospital

🇯🇵

Aichi, Japan

National Hospital Organization Kyushu Medical Center

🇯🇵

Fukuoka, Japan

Hiroshima University Hospital

🇯🇵

Hiroshima, Japan

Hyogo Brain and Heart Center

🇯🇵

Hyōgo, Japan

Kitaharima medical center

🇯🇵

Hyōgo, Japan

Odawara Cardiovascular Hospital

🇯🇵

Kanagawa, Japan

Hirosaki Stroke and Rehabilitation Center

🇯🇵

Aomori, Japan

Hirosaki University Hospital

🇯🇵

Aomori, Japan

Kimitsu Chuo Hospital

🇯🇵

Chiba, Japan

Ogaki Municipal Hospital

🇯🇵

Gifu, Japan

Brain Attack Center Ota Memorial Hospital

🇯🇵

Hiroshima, Japan

Tenri Hospital

🇯🇵

Nara, Japan

Kyorin University Hospital

🇯🇵

Tokyo, Japan

Hiroshima City Hiroshima Citizens Hospital

🇯🇵

Hiroshima, Japan

Seisho Hospital

🇯🇵

Kanagawa, Japan

Okayama Red Cross Hospital

🇯🇵

Okayama, Japan

Saitama Medical Center

🇯🇵

Saitama, Japan

Dokkyo Medical University Hospital

🇯🇵

Tochigi, Japan

Nippon Medical School

🇯🇵

Tokyo, Japan

Saitama Medical University International Medical Center

🇯🇵

Saitama, Japan

Jichi Medical University Hospital

🇯🇵

Tochigi, Japan

NTT Medical Center Tokyo

🇯🇵

Tokyo, Japan

Showa University Koto Toyosu Hospital

🇯🇵

Tokyo, Japan

Tsuruoka Municipal Shonai Hospital

🇯🇵

Yamagata, Japan

Teine Keijinkai Hospital

🇯🇵

Hokkaido, Japan

Hyogo College of Medicine College Hospital

🇯🇵

Hyōgo, Japan

Kumamoto Red Cross Hospital

🇯🇵

Kumamoto, Japan

Iwate Prefectural Central Hospital

🇯🇵

Morioka, Japan

National Cerebral and Cardiovascular Center

🇯🇵

Osaka, Japan

Osaka General Medical Center

🇯🇵

Osaka, Japan

National Hospital Organization Osaka National Hospital

🇯🇵

Osaka, Japan

Jikei University Hospital

🇯🇵

Tokyo, Japan

Juntendo University Hospital

🇯🇵

Tokyo, Japan

© Copyright 2025. All Rights Reserved by MedPath