the Study of STABLE_SR for Persistent Atrial Fibrillation
NCT ID: NCT01761188
Last Updated: 2013-06-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
220 participants
INTERVENTIONAL
2013-06-30
2015-01-31
Brief Summary
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* Hypothesis: our new method may be more effective than conventional strategy.
* Objectives:The primary objective of this investigation is to compare the efficacy of two different AF ablation strategies in patients with persistent AF:Study Group: CPVI plus electrophysiologic substrate ablation in the left atrium during sinus rhythm ( STABLE-SR);Control Group: conventional stepwise approach for persistent AF(CPVI + Lines +CFE) .The secondary objectives of this investigation are to evaluate and compare the safety and procedural characteristics of both groups.
* Sample size: 220
* Time line: 2013 Q1-2014 Q2
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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STABLE-SR
CPVI plus electrophysiologic substrate ablation in the left atrium during sinus rhythm ( STABLE-SR)
Ablation
electrophysiology substrate mapping is the critical difference between both groups
Control Group
conventional stepwise ablation approach for persistent AF(CPVI + Lines +CFE) .
Ablation
electrophysiology substrate mapping is the critical difference between both groups
Interventions
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Ablation
electrophysiology substrate mapping is the critical difference between both groups
Eligibility Criteria
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Inclusion Criteria
* Patients with persistent or long-lasting AF; Persistent AF will be defined as a sustained episode lasting \> 7 days and less than 1 years; Long-lasting persistent AF will be more than 1 year and less than 5 years.
* Patients must be willing and able to comply with all peri-ablation and follow-up requirements.
* Patients with atrial fibrillation will to accept the procedure of ablation.
* Patients signed the written informed consent for the study.
* Patients can endure the required follow up.
Exclusion Criteria
* Patients with contraindications to systemic anticoagulation with heparin or coumadin or a direct thrombin inhibitor.
* Patients with thromboemboli in LAA.
* Patients with left atrial size ≥ 55 mm (2D echocardiography, parasternal long-axis view).
* Patients allergic for contrast or iodine.
* Patients with the SCr \>3.5mg/dl or Ccr \< 30 ml/min
* Patients with life expectancy \< 12 months
* Patients who are in the period of pregnant
18 Years
80 Years
ALL
No
Sponsors
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Abbott Medical Devices
INDUSTRY
The First Affiliated Hospital with Nanjing Medical University
OTHER
Responsible Party
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Gang Yang
Doctor of Cardiology Department
Principal Investigators
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Minglong Chen, M.D.
Role: PRINCIPAL_INVESTIGATOR
The First Affiliated Hospital with Nanjing Medical University
Locations
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The First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China
Countries
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Central Contacts
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Facility Contacts
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References
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Yu Y, Wang X, Li X, Zhou X, Liao S, Yang W, Yu J, Zhang F, Ju W, Chen H, Yang G, Li M, Gu K, Tang L, Xu Y, Chan JY, Kojodjojo P, Cao K, Fan J, Yang B, Chen M. Higher Incidence of Asymptomatic Cerebral Emboli After Atrial Fibrillation Ablation Found With High-Resolution Diffusion-Weighted Magnetic Resonance Imaging. Circ Arrhythm Electrophysiol. 2020 Jan;13(1):e007548. doi: 10.1161/CIRCEP.119.007548. Epub 2020 Jan 14.
Yang B, Jiang C, Lin Y, Yang G, Chu H, Cai H, Lu F, Zhan X, Xu J, Wang X, Ching CK, Singh B, Kim YH, Chen M; STABLE-SR Investigators*. STABLE-SR (Electrophysiological Substrate Ablation in the Left Atrium During Sinus Rhythm) for the Treatment of Nonparoxysmal Atrial Fibrillation: A Prospective, Multicenter Randomized Clinical Trial. Circ Arrhythm Electrophysiol. 2017 Nov;10(11):e005405. doi: 10.1161/CIRCEP.117.005405.
Other Identifiers
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201201
Identifier Type: -
Identifier Source: org_study_id
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