심장 신경조절 치료를 위한 새로운 설정 알고리즘 (CS-10)
BackBeat Medical의 CNT(심장 신경 조절 요법) 페이싱 신호를 위한 새로운 설정 알고리즘의 임상 타당성
After meeting all inclusion/exclusion criteria, subjects on standard pacing with the Moderato® or Moderato Plus Implantable Pulse Generator (IPG) will be subjected to two set-up sessions for the CNT algorithm: at week 4 and at week 6 post implant. At the end of these visits, subjects will undergo a 24 ambulatory blood pressure recording after which CNT will be automatically turned OFF and standard pacing will resume.
The ambulatory data will provide the basis for a lasting CNT programming by week 8. Follow up visits will be scheduled after 3, 6, and 12 months.
연구 개요
상세 설명
This is a feasibility, pilot, interventional clinical study comparing the performance of CNT pacing signals delivered by Moderato® System or Moderato Plus using a new Setup Algorithm to the performance of the CNT pacing signals delivered by Moderato® System in a similar patient population in a previous multi-center, randomized, double blinded chronic trial (MODERATO II, described below).
Subjects meeting all eligibility criteria (detailed below) will receive a Moderato® IPG (Implantable Pulse Generator), either as a new implant or as a replacement to an existing pacemaker (visit 2). The subject will then be observed during the "Run-in Phase" for 30 days with the device programmed to deliver standard pacing therapy. During the "Run-In Phase", 3 weeks from implant (visit 3), the subjects will undergo a 24-hour Ambulatory Blood Pressure Measurement (ABPM). At the end of the "Run-in Phase" (4 weeks from implant at visit 4), eligibility for activation of CNT pacing signals will be re-established. Subjects eligibility will be determined following the result of the 24-hour ABPM conducted at week 3 from implant and office blood measurement at week 4 (inclusion criteria #5) and an assessment of change in ejection fraction from baseline using an echo measurement (exclusion criteria #5).
All subjects will undergo in visits 4 and 5 two sessions to test two different setup CNT Algorithms. One version will favor atrial pacing. The order of the setup versions will alternate, whereby subjects will start with setup version 1 or setup version 2 (see below). They will also undergo setup without the use of an algorithm, similar to the method used in the MODERATO II study.
After the "Run-In Phase", subjects meeting all eligibility criteria will undergo Setup Algorithm 1 (or 2). At the end of the visit, the Moderato® IPG will be programmed with the resulting CNT parameters to be delivered for 24 hours; after which the device will continue as a standard pacemaker with the pre-sets of the "Run-In Phase" period. Subjects will be fitted with 24 hour ABPM devices and sent home.
After two weeks (visit 5), subjects will return for the second setup visit. This time, subjects will undergo setup using the setup Algorithm version that was not used on them in the First Setup visit. They will also undergo setup without use of the algorithm, similar to the method used in the MODERATO II study. At the end of the second setup visit, the Moderato® IPG will be programmed using the resulting CNT parameters, to be delivered for 24 hours; after which the device will continue as a standard pacemaker with the pre-sets of the "Run-In Phase" period. Subjects will be fitted with 24 hour ABPM devices and sent home.
Subjects will return after two weeks for the trial CNT activation visit (visit 6). Based on the effect of the previous test CNT activations on blood pressure established by the two ABPM assessments, the investigator will decide whether to Continue CNT for the patient, with the parameters determined by the first or the second Setup Algorithm, or use the parameters established during setup without use of the algorithm.
Subjects will be further followed 3, 6 and 12 months post CNT activation (5, 8 and 14 months from implant) for changes in blood pressure and any adverse events (see study duration below).
At the end of the follow-up period, the treating physician will decide whether to leave CNT therapy on or off. Patient care will continue according to existing best practices.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Linda Korthout
- 전화번호: +41783482383
- 이메일: lkorthout@orchestrabiomed.com
연구 장소
-
-
-
Prague, 체코, 15030
- 모병
- Nemocnice Na Homolce (Na Homolce Hospital)
-
연락하다:
- Petr Neužil,, Prof.Dr.
- 이메일: pneuzil@seznam.cz
-
-
-
-
-
Krakow, 폴란드, 30-688
- 빼는
- Jagiellonian University Hospital
-
Poznan, 폴란드, 61-848
- 아직 모집하지 않음
- Uniwersytecki Szpital Kliniczny w Poznaniu
-
연락하다:
- Przemysław Mitkowski, Dr.
-
Szczecin, 폴란드, 72 70-111
- 아직 모집하지 않음
- Samodzielny Pub. Szpital Kliniczny nr 2 PUM
-
연락하다:
- Jaroslaw Kazmierczak, Prof. Dr.
-
Warsaw, 폴란드, 02-097
- 아직 모집하지 않음
- Publiczny Centralny Szpital
-
연락하다:
- Marcin Grabowski, Prof. Dr.
-
Zabrze, 폴란드, 41-800
- 모병
- Silesian Center for Heart Diseases
-
연락하다:
- Adam Sokal, Dr.
-
-
-
-
-
Budapest, 헝가리, 1122
- 모병
- Semmelweis University Heart and Vascular Center
-
연락하다:
- Béla Merkely, Prof.
- 전화번호: +36 1 458 6842
- 이메일: merkely.bela@kardio.sote.hu
-
연락하다:
- Istvan Osztheimer, MD
- 전화번호: +36 20 6632487
- 이메일: osztheimer.istvan@kardio.sote.hu
-
수석 연구원:
- Béla Merkely, Prof.
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Subject is ≥ 18 years of age
- Subject requires implantation or replacement of a dual chamber pacemaker or requires an upgrade from a single chamber to a dual chamber pacemaker.
- Subject has stable (for prior 1 month) hypertension treatment with 1, 2 or 3 antihypertensive drugs, which is planned to be maintained without changes for a period of at least 2 months post implant.
- Subject has an office systolic blood pressure (oSBP) ≥140 and <180 mmHg
- At 4 weeks from device implant, subject has an average 24-Hour ambulatory systolic blood pressure (aSBP) ≥130 mmHg and <170 mmHg and an office blood pressure (oSBP) ≥140 and <180 mmHg.
- Subject is willing and able to comply with study visits and procedures
- Subject is willing to adhere to the prescribed baseline antihypertension medical regimen for the duration of the study.
Exclusion Criteria:
- 1. Subject has a known secondary cause of HTN (e.g. renal vascular disease, hyperthyroidism, hyperaldosterone and pheochromocytoma)
- Subject has permanent atrial fibrillation
- Subject has intermittent paroxysmal atrial fibrillation/flutter with significant burden (i.e., >10% atrial fibrillation/flutter beats if available.
- Subject has an ejection fraction <50%
- Subject has a drop of > 15% (absolute) in ejection fraction from baseline to week 4
- Subject has symptoms of heart failure, NYHA Class II or greater
- Subject has mitral regurgitation ≥2+, aortic stenosis with valve area <1.0 cm2 , or is expected to need a valve repair or replacement.
- Subject has a history of stroke or TIA within 12 months or any prior stroke with a residual neurological deficit (modified Rankin Score >2+)
- Subject experienced myocardial infarction (MI) within 3 months prior to enrolment
- Subject had a cardiovascular interventional procedure or cardiovascular surgery within 6 months prior to enrolment
- Subject has hypertrophic cardiomyopathy, restrictive cardiomyopathy or interventricular septal thickness ≥15 mm
- Subject is on dialysis
- Subject has estimated glomerular filtration rate (GFR) <30 ml/min/1.73m²
- Subject has significant (>50% occlusion of left or right carotid artery) carotid artery stenosis
- Subject has a history of clinically significant untreated ventricular tachyarrhythmia or has experienced sudden cardiac arrest
- Subject has an active device-based treatment for hypertension
- Subject has an existing active cardiac device or neurostimulator (e.g., ICD, spinal cord stimulator)
- Subject has Type I Diabetes
- Subject is a member of a vulnerable population (e.g., prisoners, pregnant or lactating women, mentally disabled)
- Subject has the possibility of becoming pregnant during the conduct of the study and is not willing to use a means of contraception during the study
- Subject cannot or is unwilling to provide informed consent
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 크로스오버 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: CNT Setup Algorithm Version 1
When performing the Setup Algorithm Version 1, each subject's blood pressure is measured with a standard cuff system while the BackBeat-CNT is activated, and system parameters are varied successively according to a specified sequence or based on the blood pressure measurements obtained during previous activations of BackBeat CNT, until the Setup Algorithm is complete. The parameter values as determined by the Setup Algorithm will constitute the programming of the Moderato IPG for the 24 hour activation following setup. |
The effect of CNT on blood pressure will be obtained throughout the year long follow up period. |
|
실험적: CNT Setup Algorithm Version 2
When performing the Setup Algorithm Version 1, each subject's blood pressure is measured with a standard cuff system while the BackBeat-CNT is activated, and system parameters are varied successively according to a specified sequence or based on the blood pressure measurements obtained during previous activations of BackBeat CNT, until the Setup Algorithm is complete. The parameter values as determined by the Setup Algorithm will constitute the programming of the Moderato IPG for the 24 hour activation following setup. |
The effect of CNT on blood pressure will be obtained throughout the year long follow up period. |
|
다른: CNT therapy optimization without use of the Setup Algorithm
For this optimization procedure, each subject's blood pressure is measured with a continuous blood pressure measurement system while the BackBeat-CNT is activated, and system parameters are varied according to a specified sequence until the desired blood pressure reduction is achieved. The parameter values that provide the desired blood pressure reduction will be recorded, for possible use by the investigator following trial completion |
The effect of CNT on blood pressure will be obtained throughout the year long follow up period. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
CNT efficacy: Changes in average 24 hour systolic ambulatory blood pressure
기간: up to 12 Month follow-up visit
|
The change in the 24 hr blood pressure recording after each of the two set up sessions (week 4 and week 6) will be compared to the 24 hr ambulatory data of the control (week 3). |
up to 12 Month follow-up visit
|
|
CNT safety: Incidence of device- and treatment-related adverse and serious adverse
기간: up to 12 Month follow-up visit
|
Incidence of device- and treatment-related adverse and serious adverse events during the study. |
up to 12 Month follow-up visit
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Béla MERKELY, Prof. MD, Semmelweis University Heart and Vascular Center
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
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. .