- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07630857
Unipolar Voltage Mapping for Personalized Atrial Fibrillation Ablation (UNIQS-AF)
Unipolar Mapping for Personalized Atrial Fibrillation Ablation: An Interventional Study on Arrhythmia Maintenance and Atrial Remodeling
Atrial fibrillation (AF) is a common heart rhythm disorder. While catheter ablation is an effective treatment, many patients still experience AF recurrence after the procedure. One major reason is that the mechanisms that maintain AF are not fully understood. Research suggests that the outer layer of the heart (epicardium) may play an important role in keeping AF going. However, current mapping techniques have limitations in detecting electrical signals from both the inner and outer heart layers.
This study uses a different technique called unipolar voltage mapping, which may more accurately capture electrical signals from both heart layers. Specifically, we focus on a specific type of electrical signal called "QS potential" on unipolar mapping, which reflects breakthrough sites between the inner and outer heart layers.
In this interventional study, participants with AF undergoing catheter ablation will receive personalized ablation guided by unipolar QS-potential mapping. We aim to:
Explore the relationship between unipolar QS-potentials and AF maintenance and atrial remodeling Evaluate the effectiveness of QS-potential guided personalized AF ablation
연구 개요
상태
정황
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: AIJU TIAN
- 전화번호: +8618811592092
- 이메일: taj2015@163.com
연구 장소
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Beijing Municipality
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Beijing, Beijing Municipality, 중국, 100037
- 모병
- Fuwai Hospital
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연락하다:
- Jiaju Li
- 전화번호: +8618236955005
- 이메일: jiajv_li@163.com
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Age ≥ 18 years and ≤ 80 years
- Documented diagnosis of atrial fibrillation (paroxysmal or persistent)
- Planned to undergo catheter ablation for AF (including patients with recurrent AF after prior ablation)
- Able and willing to provide written informed consent
- Able to complete scheduled follow-up visits (3 months post-ablation)
Exclusion Criteria:
- Left ventricular ejection fraction < 35%
- Severe valvular heart disease (moderate to severe mitral stenosis or regurgitation)
- History of intracardiac thrombus
- Contraindication to anticoagulation
- Active infection or sepsis
- Pregnancy or breastfeeding
- Life expectancy < 12 months due to comorbid conditions
- Participation in another interventional clinical trial within 30 days prior to enrollment
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: QS-Guided Ablation Group
Participants in this arm undergo catheter ablation for atrial fibrillation guided by unipolar QS-potential mapping.
Ablation is delivered to these identified target sites in addition to standard pulmonary vein isolation.
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Participants in this arm undergo catheter ablation for atrial fibrillation guided by unipolar QS-potential mapping.
Intracardiac unipolar voltage mapping is performed to identify QS-potentials, which reflect epicardial-endocardial breakthrough sites.
Ablation is delivered to these identified target sites in addition to standard pulmonary vein isolation.
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다른: Conventional PVI Group
Participants in this arm undergo conventional pulmonary vein isolation for atrial fibrillation using standard bipolar voltage mapping.
Ablation is performed to achieve electrical isolation of the pulmonary veins, without additional mapping-guided ablation beyond PVI.
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Participants in this arm undergo conventional pulmonary vein isolation for atrial fibrillation using standard bipolar voltage mapping.
Ablation is performed to achieve electrical isolation of the pulmonary veins, without additional mapping-guided ablation beyond PVI.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Freedom from Atrial Fibrillation Recurrence at 3 Months Post Ablation
기간: 3 months (from month 1 to month 6 post-ablation)
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Freedom from any episode of atrial fibrillation (AF), atrial tachycardia (AT), or atrial flutter (AFL) lasting ≥30 seconds, as detected by electrocardiogram (ECG) or 24-hour Holter monitoring, after a 3-month blanking period following the ablation procedure.
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3 months (from month 1 to month 6 post-ablation)
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Total ablation time
기간: Intraoperative (on the day of the ablation procedure)
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Total duration of radiofrequency energy delivery during the ablation procedure, measured in minutes.
This includes all ablation applications (both pulmonary vein isolation and additional lesion sets) from the first to the last energy application.
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Intraoperative (on the day of the ablation procedure)
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
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. .