Novel Stimulation Patterns to Improve the Effectiveness of Spinal Cord Stimulation
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 43
- 试验地点
- 2
- 主要终点
- Change in Patient responder rate
研究概览
简要总结
The goal of this study is to compare pain outcomes achieved by spinal cord stimulation (SCS) using time varying stimulation patterns with pain outcomes achieved by current standard of care SCS.
详细描述
The researchers will conduct a traditional exploratory feasibility study using an investigational device to compare the clinical outcomes using time varying pulse (TVP) waveforms against time-invariant pulse (TIP) waveforms using both paresthesia and paresthesia-free SCS therapies. The therapy longevity of TVPs and TIPS will also be evaluated by tracking therapy efficacy through a long-term follow-up phase, using multiple pain assessments and at-home digital data collection.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Ability to provide informed consent
- •Chronic pain of the trunk and/or limbs for at least 6 months
- •Baseline average daily overall pain score of >60 (on a scale of 0-100mm) on the Visual Analog Scale related to pain of the back and/or limbs
- •Failed ≥3 medically supervised treatments (i.e. pain medications, physical therapy, facet joint/medial branch nerve blocks, acupuncture), and treatment with >2 classes of medications
- •Stable pain-related medication regimen 4 weeks prior to the trial. Patients will be asked to not increase or add pain-related medication during the study period
- •No back surgery within 6 months prior to Screening
- •Consumed an average total daily morphine equivalent of ≤200 mg during the 30 days prior to Screening.
- •Baseline Oswestry Disability Index score ≥40 and ≤80
- •Eligible candidate for SCS from a psychological and psychiatric standpoint as determined within 180 days prior to Baseline Visit, per site's routine screening process
- •Able to independently read and complete all questionnaires and assessments provided in English
- •Female candidates of child-bearing potential agree to use contraception during the study period
- •Deemed to be a good candidate for spinal cord stimulation by the PI, and a board certified pain management physician
- •Willing to cooperate with study requirements
排除标准
- •Patient exhibits catastrophization based on physician evaluation (e.g., average overall daily pain intensity of 100 on a 0-100mm visual analog scale, every day during the 7 days prior to Screening, based on patient recall
- •Pain originating from peripheral vascular disease
- •Active treatment for cancer in past 6 months
- •Involved in disability litigation
- •High surgical risk including documented history of allergic response to titanium or silicone, current systemic infection, or local infection in close proximity to anticipated surgical field
- •Body mass index ≥ 45 at Screening
- •Terminal illness with anticipated survival < 12 months
- •Participant is immunocompromised
- •Significant cognitive impairment at Screening that, in the opinion of the Investigator, would reasonably be expected to impair the study candidate's ability to participate in the study
- •Participating (or intends to participate) in another drug or device clinical trial that may influence the data that will be collected for this study
- •Previous spinal cord stimulation trial/implant or is already implanted with an active implantable device(s) (e.g. drug pump, implantable pulse generator)
- •A pregnant female or a female of childbearing potential planning to get pregnant during the course of the study
- •Plan to receive any massage or manipulation directly over the leads or by the anticipated location of the IPG or treatments that involve sudden jerking motions of the torso at any
- •Existing medical condition that is likely to require the use of diathermy
- •Any injury or medical/psychological condition that might be significantly exacerbated by the implant surgery or the presence of an implantable stimulator or otherwise compromise subject safety
- •Unable to operate the study devices including wrist-worn biosensor and mobile app
- •Documented history of substance abuse or dependency in the 6 months prior to baseline
结局指标
主要结局
Change in Patient responder rate
时间窗: Patient responder rate will be measured from the baseline and during three experimental stimulation periods which are 8±3 weeks each.
The primary endpoint for this trial will be a comparison of the percentage of patients achieving at least a 50% reduction in pain during the TIP stimulation block with the percentage of patients achieving at least a 50% reduction in pain during either TVP stimulation block.
次要结局
未报告次要终点
研究者
Ashwin Viswanathan
Professor
Baylor College of Medicine