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LBBP + CSP Versus LBBP Alone for Cardiac Resynchronization Therapy (LOTTO-CRT)

2026년 7월 22일 업데이트: Clinica Cardio VID

Left Bundle Branch Pacing + Coronary Sinus Pacing Versus Left Bundle Branch Pacing Alone for Cardiac Resynchronization Therapy in Patients Eligible for CRT-P A Randomized Crossover Pilot Clinical Trial

The purpose of this pilot clinical trial is to evaluate whether a novel cardiac resynchronization strategy, called LOT-CRT, is more effective than standard physiological pacing alone (LBBAP) in patients with heart failure.

This is a randomized, single-center, crossover pilot study involving 10 patients. All participants will receive a specialized pacemaker (CRT-P) with leads implanted in two specific areas: the Left Bundle Branch Area (LBBAP) and the Coronary Sinus (CS).

Because of the crossover design, each patient will serve as their own control, receiving two different pacing configurations in a random order: Active Phase (LOT-CRT): Simultaneous pacing of the left bundle branch and the coronary sinus. Control Phase (LBBAP alone): Pacing only the left bundle branch area. Each treatment phase will last 6 months, for a total follow-up of 12 months per patient.

By testing both strategies in the same patient, this study will help clinicians identify the most effective way to restore heart synchrony and improve clinical outcomes in patients with advanced heart failure and conduction delays.

연구 개요

상세 설명

This is a single-center, randomized, crossover pilot clinical trial. Each patient will serve as their own control. Following the successful implantation of a device capable of stimulating the LBBAP and the coronary sinus, participants will be randomly assigned to one of two treatment sequences:

Sequence A: LOT-CRT (LBBAP + CS) for 6 months, followed by LBBAP alone Sequence B: LBBAP alone for 6 months, followed by LOT-CRT Each treatment phase will last 6 months, followed by an end-point evaluation and a crossover. Since the hemodynamic effect of electrical stimulation is immediate, no washout period is required between phases.

This study was designed as an exploratory pilot study; therefore, no formal sample size calculation was performed. The number of patients enrolled is considered adequate to assess the feasibility of the procedure, the safety of the crossover design, and to identify preliminary signals of clinical and electrical efficacy.

연구 유형

중재적

등록 (추정된)

10

단계

  • 해당 없음

연락처 및 위치

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

연구 장소

    • Antioquia
      • Medellín, Antioquia, 콜롬비아, 050036
        • Clinica CardioVID

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. Age ≥18 years
  2. Standard CRT-P indications according to ESC 2021 (EF ≤50%, QRS ≥130 ms, sinus rhythm or controlled AF)
  3. NYHA class II-IV
  4. Coronary venous anatomy suitable for placement of a coronary sinus electrode.
  5. Signed informed consent.
  6. Successful implantation of electrodes in the coronary sinus and in the left bundle branch area (LBBAP)

Exclusion Criteria:

  1. Concomitant indication for implantation of an implantable cardioverter-defibrillator (ICD) or CRT-D
  2. Significant uncorrected valvular disease or scheduled or anticipated cardiac surgery during the study period.
  3. Anatomical or technical contraindication for lead implantation in the coronary sinus or for lead implantation in the coronary sinus (such as sinus stenosis, coronary sinus branches unsuitable for cannulation, inability to advance and/or stabilize the lead, among others)
  4. Persistent atrial fibrillation with uncontrolled rate
  5. Comorbidities that may limit life expectancy to <1 year
  6. Participation in another clinical trial that could confound the evaluation of results within the last 6 months.
  7. Pregnancy or inadequate contraception
  8. In the researcher's opinion, the participant would not comply with the activities and visits outlined in the study protocol

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: 크로스오버 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: Sequence A
LOT-CRT (LBBAP + CS) for 6 months, followed by LBBAP alone

The CS lead will be implanted in a posterolateral or lateral vein using venography and standard IV delivery sheaths. Proper lead placement is confirmed by stable fixation, pacing capture, and absence of diaphragmatic pacing.

The configuration for each phase of the study (LOT-CRT or LBBAP alone) will be assigned during randomization.

다른 이름들:
  • LOT-CRT
  • Left bundle branch block pacing + coronary sinus pacing
  • LBBAP + CS
  • LOT-CRT Strategy
  • Combined stimulation
  • Maximized electrical resynchronization

The LBBAP lead will be implanted via a transvenous approach using the C315His sheath, targeting the left bundle branch area in the right ventricular septum, ideally between the basal septum and the mid-septal region.

Criteria for confirming successful LBBAP capture will include:

  • Evidence of narrowing of the stimulated QRS complex compared to baseline.
  • Right bundle branch block morphology on the ECG-stimulus-to-R-wave time in V6 <80 ms (if available).
  • Low and stable pacing threshold (<1.5 V @ 0.4 ms).
  • Unipolar impedance between 400-1500 ohms. The CS lead will be implanted in a posterolateral or lateral vein using venography and standard IV delivery sheaths. Proper lead placement is confirmed by stable fixation, pacing capture, and absence of diaphragmatic pacing.
다른 이름들:
  • Stimulation of the left branch only
활성 비교기: Sequence B
LBBAP for 6 months only, followed by LOT-CRT

The CS lead will be implanted in a posterolateral or lateral vein using venography and standard IV delivery sheaths. Proper lead placement is confirmed by stable fixation, pacing capture, and absence of diaphragmatic pacing.

The configuration for each phase of the study (LOT-CRT or LBBAP alone) will be assigned during randomization.

다른 이름들:
  • LOT-CRT
  • Left bundle branch block pacing + coronary sinus pacing
  • LBBAP + CS
  • LOT-CRT Strategy
  • Combined stimulation
  • Maximized electrical resynchronization

The LBBAP lead will be implanted via a transvenous approach using the C315His sheath, targeting the left bundle branch area in the right ventricular septum, ideally between the basal septum and the mid-septal region.

Criteria for confirming successful LBBAP capture will include:

  • Evidence of narrowing of the stimulated QRS complex compared to baseline.
  • Right bundle branch block morphology on the ECG-stimulus-to-R-wave time in V6 <80 ms (if available).
  • Low and stable pacing threshold (<1.5 V @ 0.4 ms).
  • Unipolar impedance between 400-1500 ohms. The CS lead will be implanted in a posterolateral or lateral vein using venography and standard IV delivery sheaths. Proper lead placement is confirmed by stable fixation, pacing capture, and absence of diaphragmatic pacing.
다른 이름들:
  • Stimulation of the left branch only

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Compare the effects of the LOT-CRT strategy versus left bundle branch block pacing (LBBAP) alone in each patient, comparing baseline to the end of the study FEVI, quality of life and functional class by NYHA.
기간: 12 months
Investigators will evaluate the following parameters in each patient: Left ventricular ejection fraction (LVEF) by echocardiography and electrocardiogram; functional capacity (NYHA class) using the 6-minute walk test and symptoms reported by the patient; quality of life (MLHFQ) using the MLHFQ quality of life scale
12 months

2차 결과 측정

결과 측정
측정값 설명
기간
Change in end-systolic diameter
기간: 12 months
Absolute (mm) and relative (%) change in LVESV between baseline and 6 months.
12 months
QRS Duration
기간: 12 months
Absolute (ms) and relative (%) changes in the 12-lead ECG.
12 months
Change in end-diastolic diameter
기간: 12 months
Absolute (mm) and relative (%) change in LVEDV between baseline and 6 months.
12 months
NT-proBNP
기간: 12 months
Absolute (ng/mL) and relative (%) change in NT-proBNP from baseline to 6 months
12 months
Echocardiographic responder
기간: 12 months
LVEF ≥10% elevation or LVESV ≥15% decreased
12 months
Echocardiographic super-responder
기간: 12 months
LVEF ≥50% or LVESV ≥30% decrease
12 months
Composite Clinical Outcome
기간: 12 months
Cardiovascular Death or Hospitalization for Heart Failure
12 months
Procedural parameters
기간: 12 months
Thresholds, P- and R-waves, impedance of each electrode.
12 months
Procedure Time/Fluoroscopy
기간: 12 months
Total procedure time in minutes/ total fluoroscopy time in minutes.
12 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Juan F Agudelo, Electrophysiologist, Clinica CardioVID
  • 연구 책임자: Susana Rios, Medical Epidemiologist, Clinica CardioVID

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

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 (실제)

2026년 6월 9일

기본 완료 (추정된)

2027년 7월 1일

연구 완료 (추정된)

2027년 12월 1일

연구 등록 날짜

최초 제출

2026년 5월 26일

QC 기준을 충족하는 최초 제출

2026년 6월 17일

처음 게시됨 (실제)

2026년 6월 24일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 23일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 22일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • Clinica CardioVID
  • ERP -2025-14209 (기타 보조금/기금 번호: Medtronic)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

Individual participant data, appropriately anonymized, that support the reported results will be made available to qualified researchers for the purposes of scientific research or meta-analysis. Requests must be addressed to the Principal Investigator and include a formal proposal. All requests will be subject to approval by the institutional ethics committee. As this is a study with a small sample size (10 patients), the protocol strictly enforces confidentiality; therefore, prior approval is always required to share these data.

The data will be available from 6 months to 5 years following the publication of the main results.

IPD 공유 기간

The data will be available from 6 months to 5 years following the publication of the main results.

IPD 공유 액세스 기준

Requests must be addressed to the Principal Investigator and include a formal proposal. All requests will be subject to approval by the institutional ethics committee.

IPD 공유 지원 정보 유형

  • 연구_프로토콜
  • 수액
  • CSR

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

예

미국에서 제조되어 미국에서 수출되는 제품

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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