- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07795541
OPTImizing Lead Placement in Patients Requiring Pacemaker After Cardiac Surgery (OPTI-PACS)
OPTIMIZING LEAD PLACEMENT IN PATIENTS REQUIRING PACEMAKER AFTER CARDIAC SURGERY
Conventional right ventricular pacing has been associated with ventricular dyssynchrony and an increased risk of pacing-induced cardiomyopathy, which may lead to worse clinical outcomes. To lessen the burden of pacing-induced cardiomyopathy, the adoption of conduction system pacing has increased in recent years. In patients with normal cardiac function, measured as left ventricular ejection fraction, the superiority of conduction system pacing is less clear. As a result, both pacing strategies remain in widespread clinical use.
Patients undergoing cardiac surgery represent a vulnerable cohort for pacing-induced cardiomyopathy, given their established structural heart disease, and postoperative atrioventricular block remains a common occurrence in these patients.
This multicenter randomized trial aims to evaluate the use of conduction system pacing, in the form of left bundle branch area pacing, versus conventional pacing in patients with normal left ventricular ejection fraction after cardiac surgery.
연구 개요
상태
상세 설명
A high percentage of ventricular pacing increases the risk of pacing-induced cardiomyopathy. Pacing-induced cardiomyopathy is a syndrome defined by left ventricular dysfunction secondary to chronic right ventricular pacing, resulting in impaired outcomes. Pacing-induced cardiomyopathy is estimated to affect approximately 10-20% of patients with a high proportion of right ventricular pacing (>20%), a population that mainly consists of patients with atrioventricular block (AVB). The abnormal activation leads to prolonged electrical and mechanical activation, which results in ventricular dyssynchrony. Other important risk factors for pacing-induced cardiomyopathy include structural heart disease and reduced ejection fraction, male sex and wide, paced QRS.
Clinical practice guidelines support pacemaker implantation following cardiac surgery only for severe and non-transient bradyarrhythmias, as pacemaker implantation increases the risk of severe infections and device-related long-term complications. Evidence suggests that a substantial proportion of patients who receive a pacemaker following cardiac surgery have limited need for pacing at long-term follow-up. Thus, the risk/benefit ratio for patients following cardiac surgery differs from that of the general population, while these patients also form a vulnerable population at high risk for pacing-induced cardiomyopathy.
Over the last decade, a conduction system pacing strategy called left bundle branch area pacing (LBBAP) has been developed. In LBBAP, the pacemaker lead is inserted deep into the interventricular septum from the right ventricle to the left ventricular endocardium, targeting the left bundle and its resulting fascicles. As the current understanding of the development of pacing-induced cardiomyopathy suggests that the electrical dyssynchrony introduced by right ventricular pacing plays a crucial role, our hypothesis is that its incidence could be reduced by the favorable electrical activation achieved with LBBAP.
There are ongoing randomized controlled trials of conduction system pacing in the general population; however, none are investigating cardiac surgery patients. These patients differ substantially from the general population in age, expected long-term survival, and cardiovascular health. This increases their risk of pacing-induced cardiomyopathy and could influence the feasibility of conduction system pacing due to their otherwise impaired cardiovascular health. At the same time, their long-term pacing dependence could differ from that of the general population.
Therefore, the aim of the present multicenter randomized controlled trial is to evaluate the long-term outcomes of LBBAP versus right ventricular pacing after cardiac surgery in patients with normal left ventricular ejection fraction. A secondary aim is to assess the feasibility of LBBAP after cardiac surgery with regard to implantation success and long-term electrical parameters. The results of this trial are anticipated to provide clinically meaningful evidence to guide pacing strategy selection in this patient cohort.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Andreas S Martinsson, MD, PhD
- 전화번호: +46313427717
- 이메일: andreas.s.martinsson@vgregion.se
연구 연락처 백업
- 이름: Alice David, MD
- 전화번호: +313429684
- 이메일: laura.david@vgregion.se
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- High degree atrioventricular block
- Cardiac surgery within 30 days of pacemaker implantation
- Written informed consent
- Current left ventricular ejection fraction at or above 50%
Exclusion Criteria:
- Any concomitant condition that results in a life expectancy of less than 1 year
- Planned for heart transplant or left ventricular assist device
- Current dialysis
- Not suitable according to the opinion of the investigators due to characteristics that interfere with the adherence to the study protocol.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
활성 비교기: Conventional pacing strategy
This arm will receive a conventional pacemaker lead if they have atrioventricular block after cardiac surgery
|
Conventional pacing strategy
|
|
실험적: Left bundle branch area pacing strategy
This arm will receive a left bundle branch area pacing pacemaker lead if they have atrioventricular block after cardiac surgery
|
Conventional pacing strategy versus conduction system pacing strategy in the form of left bundle branch area pacing
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in left ventricular ejection fraction
기간: 1 year
|
Change in left ventricular ejection fraction between enrollment and end of follow-up
|
1 year
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
모든 원인으로 인한 사망
기간: 일년
|
모든 원인으로 인한 사망
|
일년
|
|
Change in left ventricular end-diastolic diameter
기간: 1 year
|
Change in LVEDD from enrollment to end of study follow-up
|
1 year
|
|
Clinical endpoints - composite
기간: 1 year
|
Composite of all-cause mortality, heart failure hospitalization, device-related hospitalization
|
1 year
|
|
Heart failure hospitalization
기간: 1 year
|
Heart failure hospitalization
|
1 year
|
|
Device-related hospitalization
기간: 1 year
|
Device-related hospitalization
|
1 year
|
|
Quality-of-life measurement
기간: 1 year
|
Quality-of-life measurement by standardized questionnaire
|
1 year
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Andreas S Martinsson, MD, PhD, Sahlgrensa university hospital
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 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 2025-08652-01
- 2025 (미국 NIH 보조금/계약: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 20241208 (기타 보조금/기금 번호: Swedish Heart- Lung Foundation)
- ALFGBG-977905 (기타 보조금/기금 번호: ALF Agreement (Swedish state))
- ALFGBG-1029431 (기타 보조금/기금 번호: ALF Agreement (Swedish state))
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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