Quantitative Superior Vena Cava Isolation in Addition to Pulmonary Vein Isolation for Paroxysmal Atrial Fibrillation
NCT ID: NCT05908955
Last Updated: 2025-02-14
Study Results
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Basic Information
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RECRUITING
NA
290 participants
INTERVENTIONAL
2024-03-17
2025-12-31
Brief Summary
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The goal of this prospective, randomized controlled trial is to test the efficacy and safety of quantitative SVCI in addition to PVI in PAF. Participants with PAF will be randomly assigned to either PVI group or PVI+ quantitative SVCI group in a 1:1 ratio and will be followed up for 12 months. The main questions it aims to answer are:
1. Evaluate the efficacy of PVI+SVCI guided by quantitative AI.
2. Assess the safety of PVI+SVCI guided by quantitative AI.
The primary end point is treatment success at 3 months after the index ablation. The secondary end points include treatment success at 12 months, and safety outcomes.
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Detailed Description
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Nevertheless, results from previous studies that evaluate the efficacy of SVCI showed conflicting results. One possible explanation is that SVC is adjacent to critical anatomy structures (such as the sinus node and the phrenic nerve), which raises safety concerns and often leads to inadequate ablation.
Therefore, it is necessary to establish standardized ablation procedure for SVCI, ensuring both safety and efficacy. To address this issue, we proposed the concept of "quantitative ablation for SVCI." By introducing AI as a quantitative measure, it is possible to achieve precise catheter ablation while minimizing the risk of procedure-related complications.
The SCORE trial is single-center, prospective, randomized controlled trial aiming to enroll 290 patients with PAF. Participants with PAF will be randomly assigned to either PVI group or PVI+ quantitative SVCI group in a 1:1 ratio, and will be followed up for 12 months. The goal is to determine whether quantitative SVCI could improve clinical results for PAF when added to PVI. The key objectives are as follows:
1. Evaluate the efficacy of PVI+SVCI guided by quantitative AI.
2. Assess the safety of PVI+SVCI guided by quantitative AI.
The primary endpoint of the study is treatment success, defined as freedom from AF, atrial flutter, or atrial tachycardia lasting longer than 30 seconds, at the 3-month follow-up. Secondary endpoints include treatment success at the 12-month follow-up and safety outcomes, including death, stroke/TIA, pericardial tamponade or effusion requiring drainage, pulmonary vein stenosis, superior vena cava stenosis, diaphragmatic nerve injury or paralysis, sinus node dysfunction, and atrial esophageal fistula.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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PVI
Participants in this group will receive pulmonary vein isolation.
PVI
pulmonary vein isolation
PVI+SVCI
Participants in this group will receive superior vena cava isolation in addition to pulmonary vein isolation.
PVI+ quantitative SVCI
pulmonary vein isolation and superior vena cava isolation guided by quantitative ablation index
Interventions
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PVI
pulmonary vein isolation
PVI+ quantitative SVCI
pulmonary vein isolation and superior vena cava isolation guided by quantitative ablation index
Eligibility Criteria
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Inclusion Criteria
* Willing to undergo catheter ablation for AF.
* Age: 40-75 years old.
Exclusion Criteria
* History of any type of thoracic surgery, including cardiac surgery.
* History of malignant tumors.
* History of permanent pacemaker implantation.
* Peripherally inserted central catheter for long-term
* Heart failure (left ventricular ejection fraction ≤40% or NYHA class III\~IV).
* Sinus node dysfunction
* Allergy to contrast agents.
* Pregnancy or lactation.
* Age: \<40yrs or \>75yrs.
40 Years
75 Years
ALL
No
Sponsors
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Chinese Academy of Medical Sciences, Fuwai Hospital
OTHER
Responsible Party
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Jun Liu,MD
Principal Investigator
Principal Investigators
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Jun Liu, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Chinese Academy of Medical Sciences, Fuwai Hospital
Locations
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Chinese Academy of Medical Science, Fuwai hospital
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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References
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Zhou Z, Hu D. An epidemiological study on the prevalence of atrial fibrillation in the Chinese population of mainland China. J Epidemiol. 2008;18(5):209-16. doi: 10.2188/jea.je2008021. Epub 2008 Sep 8.
Mark DB, Anstrom KJ, Sheng S, Piccini JP, Baloch KN, Monahan KH, Daniels MR, Bahnson TD, Poole JE, Rosenberg Y, Lee KL, Packer DL; CABANA Investigators. Effect of Catheter Ablation vs Medical Therapy on Quality of Life Among Patients With Atrial Fibrillation: The CABANA Randomized Clinical Trial. JAMA. 2019 Apr 2;321(13):1275-1285. doi: 10.1001/jama.2019.0692.
Corrado A, Bonso A, Madalosso M, Rossillo A, Themistoclakis S, Di Biase L, Natale A, Raviele A. Impact of systematic isolation of superior vena cava in addition to pulmonary vein antrum isolation on the outcome of paroxysmal, persistent, and permanent atrial fibrillation ablation: results from a randomized study. J Cardiovasc Electrophysiol. 2010 Jan;21(1):1-5. doi: 10.1111/j.1540-8167.2009.01577.x. Epub 2009 Sep 1.
Miyazaki S, Takigawa M, Kusa S, Kuwahara T, Taniguchi H, Okubo K, Nakamura H, Hachiya H, Hirao K, Takahashi A, Iesaka Y. Role of arrhythmogenic superior vena cava on atrial fibrillation. J Cardiovasc Electrophysiol. 2014 Apr;25(4):380-386. doi: 10.1111/jce.12342. Epub 2014 Jan 6.
Santangeli P, Zado ES, Hutchinson MD, Riley MP, Lin D, Frankel DS, Supple GE, Garcia FC, Dixit S, Callans DJ, Marchlinski FE. Prevalence and distribution of focal triggers in persistent and long-standing persistent atrial fibrillation. Heart Rhythm. 2016 Feb;13(2):374-82. doi: 10.1016/j.hrthm.2015.10.023. Epub 2015 Oct 23.
Da Costa A, Levallois M, Romeyer-Bouchard C, Bisch L, Gate-Martinet A, Isaaz K. Remote-controlled magnetic pulmonary vein isolation combined with superior vena cava isolation for paroxysmal atrial fibrillation: a prospective randomized study. Arch Cardiovasc Dis. 2015 Mar;108(3):163-71. doi: 10.1016/j.acvd.2014.10.005. Epub 2015 Feb 7.
Ejima K, Kato K, Iwanami Y, Henmi R, Yagishita D, Manaka T, Fukushima K, Arai K, Ashihara K, Shoda M, Hagiwara N. Impact of an Empiric Isolation of the Superior Vena Cava in Addition to Circumferential Pulmonary Vein Isolation on the Outcome of Paroxysmal Atrial Fibrillation Ablation. Am J Cardiol. 2015 Dec 1;116(11):1711-6. doi: 10.1016/j.amjcard.2015.09.005. Epub 2015 Sep 10.
Sharma SP, Sangha RS, Dahal K, Krishnamoorthy P. The role of empiric superior vena cava isolation in atrial fibrillation: a systematic review and meta-analysis of randomized controlled trials. J Interv Card Electrophysiol. 2017 Jan;48(1):61-67. doi: 10.1007/s10840-016-0198-2. Epub 2016 Oct 14.
Higuchi K, Yamauchi Y, Hirao K, Marrouche NF. The importance of superior vena cava isolation in ablation strategy for atrial fibrillation. Curr Opin Cardiol. 2013 Jan;28(1):2-6. doi: 10.1097/HCO.0b013e32835b099b.
Zhang T, Wang Y, Liang Z, Zhao H, Han Z, Wang Y, Wu Y, Ren X. Effect of Combined Pulmonary Vein and Superior Vena Cava Isolation on the Outcome of Second Catheter Ablation for Paroxysmal Atrial Fibrillation. Am J Cardiol. 2020 Jun 15;125(12):1845-1850. doi: 10.1016/j.amjcard.2020.03.030. Epub 2020 Apr 3.
Yamashita S, Tokuda M, Isogai R, Tokutake K, Yokoyama K, Narui R, Kato M, Tanigawa S, Inada K, Matsuo S, Miyanaga S, Sugimoto K, Yoshimura M, Yamane T. Spiral activation of the superior vena cava: The utility of ultra-high-resolution mapping for caval isolation. Heart Rhythm. 2018 Feb;15(2):193-200. doi: 10.1016/j.hrthm.2017.09.035. Epub 2017 Sep 22.
Miyazaki S, Taniguchi H, Kusa S, Uchiyama T, Hirao K, Iesaka Y. Conduction recovery after electrical isolation of superior vena cava--prevalence and electrophysiological properties. Circ J. 2013;77(2):352-8. doi: 10.1253/circj.cj-12-0951. Epub 2012 Oct 23.
Guan W, Li X, Chen K, Yao Y, Liu J. Anatomical variation of femoral vessels and ultrasound-guided femoral vein puncture for catheter ablation of arrhythmias. Pacing Clin Electrophysiol. 2024 Feb;47(2):330-335. doi: 10.1111/pace.14924. Epub 2024 Jan 19.
Other Identifiers
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2023-GSP-GG-33
Identifier Type: -
Identifier Source: org_study_id
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