IRCT20120215009014N381尚未招募3 期
Effect of N-acetyl cysteine versus placebo on clinical outcomes in patients with acute radicular lumbar pain: a double-blind randomized clinical trial
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 60
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
- 18 years 至 65 years（—）
- 性别
- All
入选标准
- •Age of 18 to 65 years,
- •Acute lumbar radicular pain due to disc herniation,
- •A minimum pain intensity score of 4 or more based on the VAS,
- •A minimum functional disability score of 30 or more based on disability index questionnaire,
- •Symptoms start between the last 2 to 12 weeks,
- •Lack of proper response to NSAIDs and corticosteroids
排除标准
- •Taking herbal medications or products or other supplements in the last 3 months,
- •Spinal canal stenosis or intervertebral disc degeneration,
- •Patients with progressive and severe motor symptoms,
- •History of neuropathy for other reasons,
- •History of lumbar surgery,
- •Existence of any malignancy,
- •Pregnancy or breastfeeding,
- •Chronic liver or kidney disease,
- •Hypersensitivity to N-acetyl cysteine
研究者
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