EVOKE ECAP-Controlled Lead Placement and Programming in Chronic Pain Patients
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale (VAS), 0-100 where 0 is no pain and 100 is worst pain.
研究概览
简要总结
This study is designed to evaluate the feasibility of using intra-operative ECAP and Late-Response (LR) recordings for confirmation of activating the neuronal target of the dorsal column in a single-stage SCS lead placement procedure. The collected ECAP and LR data will be analysed post-hoc to further evaluate its utility for determining the laterality of lead placement with respect to the physiologic midline of the dorsal column.
详细描述
The primary objectives of the study will be to evaluate the feasibility of using intra-operative ECAP and LR recordings for confirming the activation of the neural target of the dorsal column in a single-stage SCS lead placement procedure. The collected ECAP and LR data will be analysed post-hoc to further evaluate its utility for determining the laterality of lead placement with respect to the physiologic midline of the dorsal column. Change in pain intensity (Visual Analogue Scale = VAS) will be evaluated after 3-months of the targeted (primary) pain area.
Conventional open-loop SCS devices produce paraesthesia (a tingling sensation) that overlap the pain distribution, with the intent of masking pain perception. It is thought that conventional open-loop SCS success depends on adequacy and durability of paraesthesia coverage as well as patient tolerance of the induced sensations. For the last 40 years, the primary focus of innovation for SCS for chronic pain has been to improve the reliability of overlapping paraesthesia's with distribution of pain. Achieving adequate and stable paraesthesia coverage in the chronic pain region is known to be challenging, making back pain more difficult to treat and limiting application mostly to patients with predominant leg pain. Therefore, the use of neurostimulation for the treatment of chronic pain (especially back) shows mixed results. Declining efficacy over time has been observed in studies using low-frequency SCS programming.
Programming in the EVOKE Randomized Controlled Trial (RCT) study was performed using objective, neurophysiological feedback i.e., ECAPs for the first time since the advent of SCS to program both the control (open-loop) and test (closed-loop) chronic low back and/or leg pain patients. The trial has shown the superior long-term efficacy and durability of closed-loop SCS in treatment of chronic back and leg pain. Unpublished data collected during the study showed that objective EVOKE ECAP-based programming does not require paraesthesia overlap with pain distribution to achieve successful outcomes in low back (axial or radicular) and leg pain patients. Evaluation of data demonstrated that at 12-months follow-up (EVOKE study), 27% of subjects did not report paraesthesia in the low back region and reported 82% and 72% back pain relief with closed-loop and open-loop SCS, respectively. This is compared to 75% and 69% pain relief, respectively, in subjects who reported paraesthesia. Therefore, no interaction between the treatment effect and paraesthesia (p = 0.775) exist (EVOKE study).
The secondary objective of this observational study is to evaluate the overlap of the dermatomal pain map with the paraesthesia coverage provided by ECAP-based programming by asking the patient to report how much percentage of the primary pain area is covered by paraesthesia.
Additionally, the patients will be followed-up for 12-months and treatment outcomes (Evaluate long-term clinical outcomes (PROMIS 29+2 Profile v2.1, VAS, long-term responders in terms of pain relief, subject satisfaction with asleep lead placement, stimulation programming characteristics, neurophysiological characteristics) will be captured pre-treatment at baseline, at 3-months, 6-months and 12-months post-activation and initial programming of the closed-loop Stimulator (CLS).
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Be 18-75 years of age or older at the time of enrolment.
- •Symptoms of chronic predominant back pain for at least 6-months, with a minimum pain intensity of 5/10 in the primary pain area on VAS pain intensity questionnaire.
- •Be an appropriate candidate for the surgical procedures required in this study based on the clinical judgment of the implanting physician.
- •Be capable of subjective evaluation, able to read and understand English-written questionnaires, and able to read, understand and sign the written inform consent in English.
- •Be willing and capable of giving informed consent.
- •Be willing and able to comply with study-related requirements, procedures, and visits.
排除标准
- •Have a medical condition or pain in other area(s), not intended to be treated with SCS, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator.
- •2. Have evidence of an active disruptive psychological or psychiatric disorder or other known condition significant enough to impact perception of pain, compliance of intervention, and/or ability to evaluate treatment outcomes.
- •3. Subjects with chronic alcohol abuse or currently in rehabilitation.
- •Be benefitting within from an interventional procedure and/or surgery to treat chronic pain (Subjects should be enrolled at least 30 days from last benefit).
- •5. Have prior experience with SCS.
- •Have an existing drug pump and/or another active implantable device such as a pacemaker.
- •7. Have a condition currently requiring or likely to require the use of diathermy.
- •8. Have an active systemic or local infection at the anticipated needle entry site.
- •9. Be pregnant (if female and sexually active, subject must be using a reliable form of birth control, be surgically sterile or be at least 2 years post-menopausal).
- •10. Are currently nursing (if female).
- •11. Be concomitantly participating in another clinical study.
结局指标
主要结局
Visual Analogue Scale (VAS), 0-100 where 0 is no pain and 100 is worst pain.
时间窗: Baseline
Evaluate average pain relief using the Visual Analogue Scale (VAS).
Difference in Visual Analogue Scale (VAS), 0-100 where 0 is no pain and 100 is worst pain.
时间窗: Baseline, 3 month and 6 months
Evaluate average pain relief using the Visual Analogue Scale (VAS).Percentage change in average pain intensity in the primary region of pain on the VAS.
Difference Visual Analogue Scale (VAS), 0-100 where 0 is no pain and 100 is worst pain.
时间窗: Baseline, 3, 6 and 12 months
Evaluate average pain relief using the Visual Analogue Scale (VAS).Percentage change in average pain intensity in the primary region of pain on the VAS.
Difference in Visual Analogue Scale (VAS), 0-100 where 0 is no pain and 100 is worst pain.
时间窗: Baseline and 3 months
Evaluate average pain relief using the Visual Analogue Scale (VAS). Percentage change in average pain intensity in the primary region of pain on the VAS.
次要结局
- Pain Symptoms map.(Baseline and 12 months)
- Quality of Life and Function change using the PROMIS 29+2 Profile v2.1.(baseline to 3-months, 6-months and 12-months)
- Paraesthesia coverage dermatomal map for final programming settings.(3, 6 and 12 months)
- Quality of Life and Function change using Subject Global Impression of Change (PGIC) scale(baseline to 3-months, 6-months and 12-months)
- Quality of Life and Function change in sleep questionnaire(baseline to 3-months, 6-months and 12-months)
- Quality of Life and Function change using Satisfaction scale(baseline to 3-months, 6-months and 12-months)
- Pain Symptoms map.(Baseline)
- Pain Symptoms map.(Baseline and 3 months)
- Pain Symptoms map.(Baseline and 6 months)