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A Global Randomized Trial Evaluating the FARAFLEX™ Mapping and Pulsed Field Ablation System With Electrographic Flow Mapping in Patients Undergoing Repeat Ablation for Atrial Fibrillation (ReDEFINE-AF)

2026年9月10日 更新者:Boston Scientific Corporation
The goal of the ReDEFINE-AF Clinical Study is to evaluate the safety and effectiveness of the FARAFLEX™ Mapping and Pulsed Field Ablation System with electrographic flow mapping in subjects undergoing repeat ablation for atrial fibrillation (AF).

調査の概要

研究の種類

介入

入学 (推定)

650

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. At least 18 years old, or older if required by local law.
  2. Subjects with symptomatic atrial fibrillation who have documented Persistent Atrial Fibrillation (PersAD) or Paroxysmal Atrial Fibrillation (PAF) with at least one documented symptomatic AF episode lasting at least 24 hours.

    AND Undergone one failed endocardial atrial fibrillation ablation procedure OR undergone no more than two prior endocardial atrial fibrillation ablation procedures that were both limited to PV and/or PW ablation.

  3. Willing and capable of providing informed consent.
  4. Willing and capable of participating in all follow-up assessments and testing associated with this clinical investigation at an approved clinical investigational center.
  5. Willing to receive a LUX-Dx insertable cardiac monitor (ICM) during the study or already has a LUX-Dx ICM that was inserted within 6 months prior to consent, and willing to comply with the LUX-Dx Latitude Clarity transmission instructions.

Exclusion Criteria:

  1. Any of the following atrial conditions:

    1. Left atrial anteroposterior (LA) diameter ≥ 6.5 cm, or if LA diameter is not available, non-indexed LA volume >100 mL.
    2. Current atrial myxoma.
    3. Current left atrial thrombus.
    4. Any PV abnormality, stenosis, or stenting. Common and middle PVs are admissible.
  2. Any of the following cardiovascular conditions:

    1. History of sustained ventricular tachycardia or any ventricular fibrillation.
    2. Severe right ventricular dysfunction with documented echocardiography and/or hemodynamic data.
    3. Atrial Fibrillation (AF) that is secondary to electrolyte imbalance, thyroid disease, alcohol, or other reversible/non-cardiac causes.
    4. Presence of any of the following:

      • Current or anticipated pacemaker, implantable cardioverter defibrillator, or cardiac resynchronization therapy device.
      • Implantable loop recorder other than a LUX-Dx device
      • Interatrial baffle, atrial septal defect or patent foramen ovale closure device or patch
      • Left Atrial Appendage Closure or Occlusion Device
    5. Presence of any of the following:

      • Any cardiac valve prosthesis, ring, repair, or clip.
      • Mitral valve stenosis: moderate or greater.
      • Aortic stenosis: moderate or greater.
      • Severe mitral regurgitation.
      • Severe tricuspid regurgitation.
    6. Hypertrophic or amyloid cardiomyopathy.
    7. Any IVC filter, known inability to obtain vascular access, or other contraindication to femoral access.
    8. Awaiting cardiac transplantation or other planned cardiac surgery within the next 12 months.
  3. Any of the following conditions documented during eligibility assessment or Baseline Assessment, as applicable:

    1. Heart failure associated with NYHA Class III or IV, as documented during eligibility assessment or Baseline Assessment.
    2. Most recent documented LVEF <40% within the previous 12 months.
    3. Body Mass Index (BMI) >45.0 kg/m², as documented during eligibility assessment or Baseline Assessment.
    4. Known coagulopathy or bleeding disorder.
    5. Contraindication to, or unwillingness to use, systemic anticoagulation or acceptable alternatives pre-, intra-, and post-procedure to achieve adequate anticoagulation.
    6. Women who are confirmed to be pregnant or lactating at the time of the ablation procedure.
    7. Severe lung disease, including but not limited to severe pulmonary hypertension, involving abnormal blood gases or requiring supplemental oxygen.
    8. Active malignancy other than squamous cell carcinoma.
    9. Clinically significant gastrointestinal problems involving the esophagus or stomach, including severe or erosive esophagitis, uncontrolled gastric reflux, gastroparesis, esophageal candidiasis, or active gastroduodenal ulceration.
    10. Known active systemic infection.
    11. Predicted life expectancy of less than one year per Investigator medical judgment.
    12. Subjects who are currently enrolled in another investigational study or registry that would directly interfere with the current study, except when the subject is participating in a mandatory governmental registry or a purely observational registry with no associated treatments.
    13. Required use of phosphodiesterase inhibitors within 24 hours of the ablation procedure.
    14. Known allergic drug reaction to nitroglycerin, excluding hypotension.
    15. Unwillingness to receive, or unable to tolerate, a subcutaneous, chronically inserted LUX-Dx ICM device.
    16. Presence of an active spinal cord stimulator.
  4. Any of the following congenital conditions:

    1. Congenital heart disease with any clinically significant residual anatomic or conduction abnormality.
    2. History of known congenital methemoglobinemia.
    3. History of known G6PD deficiency.
  5. Any of the following conditions in the medical history:

    1. Solid organ or hematologic transplant, or currently being evaluated for a transplant.
    2. Any prior history or current evidence of hemi-diaphragmatic paralysis or paresis.
    3. Any documented history of Prinzmetal angina or severe non-revascularizable coronary disease.
    4. Renal insufficiency if an estimated glomerular filtration rate (eGFR) is <30 mL/min/1.73 m², or any history of renal dialysis or renal transplant.
    5. Any other general health condition that, in the Investigator's medical opinion, would prevent participation in the study, interfere with assessment or therapy, significantly raise the risk of study participation, or modify outcome data or its interpretation.
  6. Any of the following events within 90 days prior of the consent date:

    1. Myocardial infarction, unstable angina, or coronary intervention.
    2. Any cardiac surgery.
    3. Heart failure hospitalization.
    4. Pericarditis or symptomatic pericardial effusion.
    5. Gastrointestinal bleeding.
    6. Stroke, TIA, or intracranial bleeding.
    7. Any active non-neurologic thrombus and/or thromboembolic event.
    8. Carotid stenting or endarterectomy.
    9. Uncontrolled diabetes mellitus or a recorded HbA1c >8.0%.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Treatment Arm
Subjects will undergo EGF mapping using the OptiMap™ Catheter and System, followed by ablation of eligible EGF-identified extra-pulmonary vein sources using the FARAFLEX™ Mapping and PFA System.
Catheter used for electrophysiological mapping of cardiac structures and the treatment of paroxysmal or persistent atrial fibrillation.
アクティブコンパレータ:Control Arm
Subjects will undergo EGF mapping using the OptiMap™ Catheter and System; however, investigators and laboratory staff will remain blinded to EGF source maps until completion of the Index Procedure, and EGF-identified sources will not be ablated. For Control Arm subjects who have not previously undergone posterior wall ablation/isolation and who do not have documented durable posterior wall isolation, protocol-defined de novo posterior wall ablation will be performed using the FARAFLEX™ Mapping and PFA System.
Catheter used for electrophysiological mapping of cardiac structures and the treatment of paroxysmal or persistent atrial fibrillation.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
The Primary Effectiveness Endpoint (PEE) is the Proportion of Randomized Subjects in the Main Study Cohort achieving Treatment Success through the Day 365 Assessment.
時間枠:Day 180 through Day 365 Assessment
The Primary Effectiveness Endpoint analysis will compare Treatment Success between the Treatment Arm and the Control Arm in randomized subjects in the Main Study Cohort.
Day 180 through Day 365 Assessment

二次結果の測定

結果測定
メジャーの説明
時間枠
The Secondary Safety Endpoint is the rate of protocol-defined device- or procedure-related Composite Serious Adverse Events (CSAE).
時間枠:Day 0 through Day 60
The secondary safety endpoint will be evaluated in Randomized Treatment Arm subjects and will not contribute to study success criteria.
Day 0 through Day 60

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月1日

一次修了 (推定)

2029年7月1日

研究の完了 (推定)

2031年7月1日

試験登録日

最初に提出

2026年9月10日

QC基準を満たした最初の提出物

2026年9月10日

最初の投稿 (実際)

2026年9月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月15日

QC基準を満たした最後の更新が送信されました

2026年9月10日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

はい

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