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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)

2026년 9월 10일 업데이트: 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).

연구 개요

연구 유형

중재적

등록 (추정된)

650

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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%.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
활성 비교기: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
The Primary Effectiveness Endpoint (PEE) is the Proportion of Randomized Subjects in the Main Study Cohort achieving Treatment Success through the Day 365 Assessment.
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
The Secondary Safety Endpoint is the rate of protocol-defined device- or procedure-related Composite Serious Adverse Events (CSAE).
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 11월 1일

기본 완료 (추정된)

2029년 7월 1일

연구 완료 (추정된)

2031년 7월 1일

연구 등록 날짜

최초 제출

2026년 9월 10일

QC 기준을 충족하는 최초 제출

2026년 9월 10일

처음 게시됨 (실제)

2026년 9월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 10일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

예

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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