EUCTR2022-003925-23-BE招募中1 期
Pain medication tapering for patients with Persistent Spinal PainSyndrome Type II, treated with Spinal Cord Stimulation. - PIANISSIMO
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 195
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •- Patients being diagnosed with persistent spinal cord stimulation type 2, defined as patients suffering from neuropathic pain of radicular origin with pain in the lower back and/or leg(s), of an intensity of at least 4/10 on the Numeric Rating Scale, for a period of at least 6 months after a minimum of one anatomically successful spinal surgery and being refractory to conservative treatment (according to Belgian reimbursement rules from January 1st, 2018).
- •- Patients need to be scheduled for SCS to be eligible for participation in the study
- •- Currently taking opioids
- •- 18 years and older
- •- Speaking and reading Dutch or French
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 156
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 39
排除标准
- •- Being actively treated for cancer,
- •- Having a life expectancy below 6 months,
- •- Receiving intrathecal drug delivery,
- •- Having contraindications for Clonidine (e.g., known hypotension which requires medication) or for Buprenorphine/Naloxone (e.g., severe respiratory insufficiency, hepatic insufficiency)
- •- Having epilepsy currently treated by Pregabalin,
- •- Currently using benzodiazepines at doses more than 40 mg diazepam-equivalents per day.
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