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the Study of STABLE_SR for Persistent Atrial Fibrillation (STABLE-SR)

Primary Purpose

Atrial Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Ablation
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Persistent Atrial fibrillation;LA substrate;ablation;voltage mapping

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing a first-time ablation procedure for AF;
  • 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 paroxysmal AF; Paroxysmal AF will be defined as a sustained episode lasting < 7days.
  • 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

Sites / Locations

  • The First Affiliated Hospital of Nanjing Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

STABLE-SR

Control Group

Arm Description

CPVI plus electrophysiologic substrate ablation in the left atrium during sinus rhythm ( STABLE-SR)

conventional stepwise ablation approach for persistent AF(CPVI + Lines +CFE) .

Outcomes

Primary Outcome Measures

Freedom from AF and/or atrial tachyarrhythmias (ATs) off antiarrhythmic drugs (AADs).
AF and/or AT occurring in the first 3 months after the ablation (blanking period) were censored.Beyond this, any symptomatic or asymptomatic AF or AT episode that lasted for more than 30 seconds was categorized as a recurrence.

Secondary Outcome Measures

total procedure time
time from puncture to the end
fluoroscopy time
total fluoroscopy time
complications
occurrence of serious adverse events that included death, pericardial effusion causing tamponade or requiring pericardiocentesis, cerebrovascular events, significant PV stenosis (symptomatic or asymptomatic ≤70% reduction in PV diameter in ≥1 veins), left atrial-esophageal fistula, diaphragmatic paralysis, and any vascular complication requiring transfusion or intervention

Full Information

First Posted
December 15, 2012
Last Updated
June 22, 2013
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Collaborators
Abbott Medical Devices
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1. Study Identification

Unique Protocol Identification Number
NCT01761188
Brief Title
the Study of STABLE_SR for Persistent Atrial Fibrillation
Acronym
STABLE-SR
Official Title
The Study of CPVI Plus Electrophysiological Substrate Ablation in the Left Atrium During Sinus Rhythm (STABLE-SR) for the Treatment of Persistent Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Unknown status
Study Start Date
June 2013 (undefined)
Primary Completion Date
July 2014 (Anticipated)
Study Completion Date
January 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University
Collaborators
Abbott Medical Devices

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background:the ablation outcomes for the treatment of persistent atrial fibrillation are not as satisfactory as paroxsymal AF. The successful rate ranges from 30%-55%. We found a new novel strategy for the modification of LA substrate during sinus rhythm based on our pilot study. 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
Detailed Description
what's is STABLE-SR approach? In our center, the LA substrate mapping was performed in patients with paroxysmal AF and persistent AF during sinus rhythm, particularly 20 normal subjects as control group as well. Our study showed that along with the duration of AF the average voltage of LA deceased and the area of low voltage zone increased. The whole activation time of entire LA would be longer. More complex fractionated electrograms was found in LA. Importantly, we identified the low voltage zone (voltage range: 0.1-0.4mV) and the transitional zone (voltage range: 0.4-1.3mV) in which most of complex fractionated electrograms located. Based on our findings a new novel ablation strategy has emerged, which is modification of LA substrate during sinus rhythm (CPVI+STABLE-SR). Our sequential protocol included 5 steps. First CPVI should be completed followed by CTI ablation to be blocked. Then if AF rhythm maintained cardioversion would be taken. High density mapping of LA substrate would be done during sinus rhythm to identify the low voltage zone and transitional zone. Linear ablation or/and spot ablation should be designed according to the mapping results. Finally bidirectional conduction block should be demonstrated for all the linear lesion and all pulmonary veins would be checked for isolation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Persistent Atrial fibrillation;LA substrate;ablation;voltage mapping

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
STABLE-SR
Arm Type
Experimental
Arm Description
CPVI plus electrophysiologic substrate ablation in the left atrium during sinus rhythm ( STABLE-SR)
Arm Title
Control Group
Arm Type
Experimental
Arm Description
conventional stepwise ablation approach for persistent AF(CPVI + Lines +CFE) .
Intervention Type
Procedure
Intervention Name(s)
Ablation
Intervention Description
electrophysiology substrate mapping is the critical difference between both groups
Primary Outcome Measure Information:
Title
Freedom from AF and/or atrial tachyarrhythmias (ATs) off antiarrhythmic drugs (AADs).
Description
AF and/or AT occurring in the first 3 months after the ablation (blanking period) were censored.Beyond this, any symptomatic or asymptomatic AF or AT episode that lasted for more than 30 seconds was categorized as a recurrence.
Time Frame
1 year after a single-ablation procedure
Secondary Outcome Measure Information:
Title
total procedure time
Description
time from puncture to the end
Time Frame
1 year
Title
fluoroscopy time
Description
total fluoroscopy time
Time Frame
1 year
Title
complications
Description
occurrence of serious adverse events that included death, pericardial effusion causing tamponade or requiring pericardiocentesis, cerebrovascular events, significant PV stenosis (symptomatic or asymptomatic ≤70% reduction in PV diameter in ≥1 veins), left atrial-esophageal fistula, diaphragmatic paralysis, and any vascular complication requiring transfusion or intervention
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing a first-time ablation procedure for AF; 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 paroxysmal AF; Paroxysmal AF will be defined as a sustained episode lasting < 7days. 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Minglong Chen, M.D.
Phone
008613809000791
Email
chenminglong2001@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Gang Yang, M.D.
Phone
008613520778385
Email
yanggangpumc@yahoo.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Minglong Chen, M.D.
Organizational Affiliation
The First Affiliated Hospital with Nanjing Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The First Affiliated Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Minglong Chen, M.D.
Phone
008613809000791
Email
chenminglong2001@163.com
First Name & Middle Initial & Last Name & Degree
Minglong Chen, M.D.
First Name & Middle Initial & Last Name & Degree
Bing Yang, M.D.

12. IPD Sharing Statement

Citations:
PubMed Identifier
31937118
Citation
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.
Results Reference
derived
PubMed Identifier
29141843
Citation
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.
Results Reference
derived

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