TCTR20230608001招募中2 期
Efficacy and Safety of the Topical Chili Extract-Loaded Lipid Nanoparticle Gel Product Containing 0.075% Capsaicin for the Treatment of Neuropathic Low Back Pain: A Randomized Controlled Trial
Bangkok Lab and Cosmetic Public Company Limited0 个研究点目标入组 100 人开始时间: 2023年6月8日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 100
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
- 年龄范围
- 20 Years 至 75 Years(—)
- 性别
- All
入选标准
- •1. Diagnosed with neuropathic low back pain, no prior back surgery.
- •2. Neuropathic pain confirmed by DN4 score of more than 4.
- •3. Age: 20-75 years at screening.
- •4. Stable pain with consistent oral therapy for more than 2 weeks.
- •5. Moderate-to-severe low back pain (PI-NRS score of more than 4 at screening).
- •6. Willing to discontinue other topical pain medications for more than 7 days during the study.
- •7. Written informed consent provided.
排除标准
- •1. Presence of severe co-morbidity, uncontrolled medical condition(s), or other illness(es) that may preclude participation.
- •2. Low back pain caused by conditions other than a neuropathic component.
- •3. Significant neurological or psychiatric disorder(s) unrelated to neuropathic pain interfering with pain assessment.
- •4. Skin condition(s) where the investigational product will be applied.
- •5. Planned elective surgery during the study period, regardless of relevance to the assessed condition.
- •6. Contraindications to capsaicin or investigational product ingredients.
- •7. Hypersensitivity history to capsaicin or investigational product ingredients.
- •8. Pregnancy, breastfeeding, or intent to conceive during the study (applies to both male and female participants).
- •9. Alcoholism or substance abuse problem(s).
- •10. Recent use of drugs, herbs, or dietary supplements that may interact with capsaicin or investigational product ingredients within 14 days of the screening visit.
- •11. Concurrent or recent participation in another clinical trial within 30 days of the screening visit.
研究者
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