Paresthesia-free Peripheral Nerve Field Stimulation for Trigeminal Neuralgia: a Double-blinded, Randomized Trial (FreeST Trial)
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 24
- 试验地点
- 4
- 主要终点
- Visual Analogue Scale (VAS) Score Change
研究概览
简要总结
Study type: Prospective, double-blinded, double arm, cross-over, randomized controlled clinical trial.
Brief protocol:
Postoperative week 0-2 -> Conventional parameters (parameters tested during trial period)
Postoperative week 2-6 -> Sham stimulation (2 weeks) and paresthesia-free stimulation (2 weeks) double-blind crossover design
Postoperative week 6 - month 12 -> Parameters that patients feel more benefit from
详细描述
Background:
Peripheral Nerve Field Stimulation (PNFS) has been utilized for the treatment of facial pain for around 60 years, and the commercial devices needed to deliver PNFS have been available for around 30 years. The safety and efficacy of the procedure has been demonstrated by various uncontrolled observational studies. It serves as a part of daily neurosurgical practice for selected patients in UHN Toronto Western Hospital. This therapeutic modality involves subcutaneous implantation of electrodes in the vicinity of trigeminal nerve branches and application of electrical current using a permanently implanted pulse generator (IPG). Similar to other forms of neuromodulation, PNFS is non-ablative, reversible, adjustable and associated with a relatively low risk of severe complications. A meta-analysis of paresthesia-inducing (PI) PFNS studies in the literature revealed a treatment efficacy of 75% decrease in VAS scores (mean difference: -6.32 out of 10) with PNFS utilization for facial pain. (PMID: 35180702)
Study design:
Patients who underwent a successful unilateral PNFS implantation surgery (trial and permanent implantation) for a facial pain syndrome as a standard of care treatment, will be screened for inclusion after permanent implantable pulse generator (IPG) implantation. Upon consent, the investigators will set up participants' IPG to deliver stimulation with parameters tested during the trial period (paresthesia-inducing parameters) for 2 weeks. The participants will come back to hospital at postoperative week 2 and will be randomized (1:1 ratio) between the two arms of the study (Group 1= sham, Group 2= paresthesia-free (PF) stimulation). Each participant will consecutively experience all two stimulation groups by 2-week periods in a crossover design. Both participants and clinical investigators that will assess the pain will be blind during the study period (between postoperative week 2 and 6). After 6 weeks, the treatment arms will be merged and all the participants will receive any stimulation parameter that they feel more benefit from ("best" parameter). Outcomes will be assessed 6 and 12 months post-operatively.
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
- Double (Participant, Outcomes Assessor)
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
- •Diagnosis of a medically-refractory unilateral facial pain syndrome as defined by the Burchiel classification but excluding atypical facial pain (somatoform pain disorder)
- •Recent successful PNFS trial and permanent implantation surgery
- •Average preoperative episodic/constant pain intensity of 5 or greater out of 10 cm on the VAS
- •Capable of providing informed consent and complying with study procedures
- •Patients may or may not use a pain medication at the time of recruitment. Medications allowed during the study are long-acting/modulatory analgesics (anticonvulsants such as carbamezapine, oxcarbazepine, pregabalin, gabapentin, lamotrigine; baclofen, botox injections) and short-acting analgesics (non-steroid anti-inflammatory drugs, short-acting opioids, lidocaine or sumatriptan injections)
排除标准
- •Currently in a clinical trial involving an investigational product or non-approved use of a drug or device.
- •Active psychiatric disorder or other known condition that can significantly impact pain perception
- •Patients with a revision surgery of a PNFS system by any reason (history of trigeminal pain surgery of other types (i.e., microvascular decompression, gamma knife, percutaneous rhizotomies) are not exclusion criteria)
- •Pregnant and lactating women
研究组 & 干预措施
Paresthesia-Free Stimulation
Duration: 2 weeks
干预措施: Paresthesia-free Peripheral Nerve Field Stimulation (Other)
Sham Stimulation
Duration: 2 weeks
干预措施: Sham stimulation (Other)
结局指标
主要结局
Visual Analogue Scale (VAS) Score Change
时间窗: Postoperative week 2 to week 6
VAS score change between sham condition (postop week 2-4 or postop week 4-6) and Paresthesia-free stimulation condition (postop week 2-4 or postop week 4-6) VAS score ranges from 0 to 100 mm (or 0 to 10 cm). Higher score is worse outcome.
次要结局
- Visual Analogue Scale (VAS) Score Change(Postoperative month 6 and 12)
- Barrow Neurological Institute (BNI) pain intensity score change(Postoperative month 6 and 12)
- Brief Pain Inventory (BPI) score change(Postoperative month 6 and 12)
- Clinician and Patient Global Impression of Change Scale and Patient satisfaction scale score change(Postoperative week 0 to week 6)
- Adverse effect Profile(Postoperative week 0 to month 12)
- Ratio of patients who chose paresthesia-free or paresthesia-inducing stimulation at week 6, month 6 and 12(Postoperative week 6, month 6 and 12)
- fMRI BOLD signal change(Between postoperative month 6 and 12)
研究者
Mojgan Hodaie
Professor
University Health Network, Toronto