Pilot Study Evaluating the Safety of Electroducer Sleeve Medical Device for Temporary Cardiac Stimulation During Percutaneous Cardiovascular Interventions, in All Kind of Patients
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Electroducer
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- To assess the peri procedural safety of ELECTRODUCER SLEEVE device used for temporary cardiac pacing during percutaneous cardiovascular interventions, by radial and femoral routes of access.
研究概览
简要总结
During percutaneous cardiovascular intervention, temporary cardiac stimulation may be required. Usually this stimulation is generated via a temporary pacing catheter. In order to reduce the complexity of the procedure, a new stimulation strategy has been developed: the "Direct Wire Pacing technique".In this approach, the cardiac stimulation is provided via the guidewire connected to an external pacemaker.
Previous study demonstrated the superiority of the new technique compared to the former. However this technique is likely to generate electrical pain, risk of bleeding for the patient and risk of blood exposure accident for the operators. This is why the medical device ELECTRODUCER SLEEVE has been developed. This device integrates a pacing function to the introducer and the guidewire used. The "Direct Wire Pacing technique" is simplified, secured and more reproducible.
详细描述
During percutaneous cardiovascular interventions such as Transcatheter Heart Valve or coronary intervention, temporary cardiac stimulation may be required. Usually this stimulation is generated via a temporary pacing catheter in the right ventricle. This procedure requires an additional venous access and the insertion of the stimulation catheter, which are both likely to generate complications. In order to reduce the complexity and increase the safety of the procedure, a new stimulation strategy has been developed: the "Direct Wire Pacing technique". In this approach, the specific venous access and the implantation of a stimulation catheter are avoided. The cardiac stimulation is provided via the guidewire inserted into the left ventricle or into the coronary arteries. This guidewire is connected to an external Pacemaker using an alligator clamp (Cathode). The Pacemaker anode is also connected using a clamp attached to a needle piercing the subcutaneous tissue, obtaining a closed electrical circuit. This technique was validated during previous studies in the TAVI context through two registries and one randomized controlled trial. This study demonstrated the superiority of the new technique by showing a reduction of the procedural duration, radiation exposure and costs; with similar efficacy and safety. However the subcutaneous needle insertion is likely to generate electrical pain, risk of bleeding for the patient and risk of blood exposure accident for the operators. This subcutaneous anode increases the stimulation threshold (mA) which can cause stimulation failures. Moreover, several technical difficulties preclude general adoption by the scientific community. This is why the medical device ELECTRODUCER SLEEVE has been developed. This device integrates a pacing function to the introducer and the guidewire used during percutaneous cardiovascular interventions. The guidewire then behaves like an intra-cardiac cathode. Thanks to the device, the complex manipulation of needles and clamps during the intervention are avoided as well as pole inversions. The "Direct Wire Pacing technique" used during the coronary and structural interventions is thus simplified, secured and more reproducible.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 99 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients ≥ 18 years old
- •Patients with a percutaneous cardiovascular intervention indication, requiring temporary cardiac stimulation
- •Procedure carried out with a 6Fr TERUMO introducer ≥ 65 mm
- •Procedure performed by femoral or radial routes
- •Patients able to understand and provide informed consent
- •Patients able to perform the planned follow-up visit one month after the procedure.
排除标准
- •Patients requiring a definitive PM
- •Pregnant or breastfeeding woman
- •Patiens under judicial protection, tutorship or curatorship
- •Negative Allen test or absence of radial pulse in the artery or vein used for intervention
- •Patient participating in another interventional clinical trial.
研究组 & 干预措施
Radial group
Use of Electroducer Sleeve on radial route
干预措施: Electroducer Sleeve (Device)
femoral group
Use of Electroducer Sleeve on femoral route
干预措施: Electroducer Sleeve (Device)
结局指标
主要结局
To assess the peri procedural safety of ELECTRODUCER SLEEVE device used for temporary cardiac pacing during percutaneous cardiovascular interventions, by radial and femoral routes of access.
时间窗: during intervention
The device safety is assessed through the occurrence of bleeding complications at the access site where the ELECTRODUCER SLEEVE was used, including: Hematoma formation (EASY Classification) and Access-site Bleeding (BARC classification).
次要结局
- To evaluate the performance of the ELECTRODUCER SLEEVE device(during intervention)
- To evaluate the patient comfort with ELECTRODUCER SLEEVE use(during intervention)
- To evaluate the occurrence of Radial Artery Occlusion(at discharge and 1 month)
- To evaluate the occurrence of allergic or adverse tissue reactions(at discharge and 1 month)
- To evaluate the impact of the ELECTRODUCER SLEEVE use on the TAVI procedure duration.(during intervention)
- To establish the efficacy of the ELECTRODUCER SLEEVE device(during intervention)
- To assess the user's overall impression of the ELECTRODUCER SLEEVE device and use.(during intervention)
