Parasternal Access for ShockS and Pacing With an acUtely Placed Less-invasive Lead for EV-ICD (PASS PULL EV-ICD) Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Incidence of SADEs
研究概览
简要总结
The PASS PULL EV-ICD Study is a prospective, multi-center, single-arm study without concurrent or historical controls. This initial concept feasibility study is primarily intended to demonstrate that the EV-ICD Lead can be safely positioned within the anterior mediastinum as intended using the AtaCor delivery system. The study will secondarily characterize the ability for the EV-ICD Lead to facilitate VF sensing and defibrillation.
详细描述
The primary objective of the study is to demonstrate that the AtaCor EV-ICD Lead can be safely positioned within the anterior mediastinum as intended using the EV-ICD Dilator and EV-ICD Delivery Tool. The study will secondarily characterize the ability for the EV-ICD Lead to facilitate VF sensing and defibrillation.
Up to 3 Investigational Sites will participate with up to 65 subjects enrolled in the study. Patients undergoing de novo or replacement ICD procedure will be eligible for participation. Study participation requires acute evaluation of the EV-ICD Lead during the index procedure. Echocardiography will be used to evaluate any new or worsening pericardial effusions. A follow-up visit will occur 7-10 days post-removal via phone, video call, or in-person. Participation will end after completion of the 7-10 days post-removal visit. The Study is expected to last up to 3 months for enrollment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •At least 18 years old
- •Indicated for de novo or replacement ICD procedure
排除标准
- •NYHA IV functional class
- •BMI ≥ 35 kg/m2
- •Inotropic therapy in past 180 days
- •Subjects with a hemodynamically unstable intrinsic heart rate that requires continual ventricular pacing
- •Presence or planned use of subcutaneous coils/arrays, epicardial patches or epicardial pace/sense leads
- •Subjects on anticoagulation/antiplatelet therapy that cannot be temporarily discontinued for the procedure
- •Logistical or safety related circumstances that may prevent data collection or follow-up
- •Participation in any concurrent clinical study without prior written approval from the Sponsor
- •Inability to give an informed consent to participate in the Study
- •Known prior history for any of the following:
- •Structural abnormalities of the heart that may increase risk of the study procedure or an obstructed/restricted pathway into the mediastinum for the EV-ICD Dilator, EV-ICD Delivery Tool and EV-ICD Lead as assessed from available CT or Echocardiography.
- •Uncontrolled paroxysmal, persistent or permanent atrial fibrillation
- •Median or partial sternotomy
- •Surgery with disruption of the lung, pericardium or connective tissue between the sternum and pericardium
- •Significant anatomic derangement of or within the thorax (e.g., pectus excavatum, significant scoliosis)
- •Thoracic radiation therapy, pneumothorax, pneumomediastinum or other medical treatments/conditions which may complicate the EV-ICD Lead insertion procedure
- •Pericardial disease, pericarditis and mediastinitis
- •Medical treatments, surgeries or conditions that increase the potential for pericardial adhesions
- •FEV1 < 1.0 Liter
- •Surgically corrected congenital heart disease (not including catheter-based procedures)
- •Allergies to the device materials as listed in the Instructions for Use (IFU)
研究组 & 干预措施
AtaCor EV-ICD Lead System
Subjects inserted with the AtaCor EV-ICD Lead Model AC-7000
干预措施: AtaCor EV-ICD Lead (Device)
结局指标
主要结局
Incidence of SADEs
时间窗: Up to 10 days post-procedure
Incidence of Serious Adverse Device Effects (SADEs)
Rate of Insertion Success
时间窗: Procedure
Defined as the ability to deploy the lead in a position within the mediastinum that is suitable for defibrillation testing and does not result in one (1) or more SADEs
次要结局
- Functionality - Lowest Defibrillation Conversion Energy(Procedure)
- Observational: Incidence of ADEs(Up to 10 days post-procedure)