JPRN-jRCTs031180436进行中(未招募)2 期
A randomized, placebo-controlled, double-blind comparative study to evaluate the efficacy of the antioxidant N-acetylcysteine (NAC) for intervertebral disc degeneration.
Watanabe Kota0 个研究点目标入组 60 人开始时间: 2019年3月27日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 进行中(未招募)
- 发起方
- 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
- >= 20age old 至 <= 64age old(—)
- 性别
- All
入选标准
- •1) Patients with lumbar disc degeneration based on images(Pfirrmann grade: 3, 4) and neurological findings
- •2) Age From 20 years old to less than 65 years old
- •3) During the study period, anti-inflammatory / analgesic agents (NSAIDs including COX-2 inhibitors, an extract from Inflamed cutaneous tissue of rabbits inoculated with Vaccinia Virus (neurotropin), antioxidant vitamin E formulation(yubera), as well as steroidal agents (oral preparation and injection)), those who agree to discontinue the use.
排除标准
- •1) Patients with complications such as severe heart, lung, liver, and blood diseases
- •2) Patients who received surgical treatment judged by the attending physician to affect the exam
- •3) Patients whose ALT / AST values before administration exceed 3 times the institution standard value
- •4) Currently, supplements containing NAC or NAC or supplements with antioxidant action (vitamin E) ingested
- •5) Patients who are allergic to drugs including NAC
- •6) Women who are pregnant, nursing, maybe pregnant or prefer pregnant during treatment
- •7) Patients who have undergone spinal surgery in the past
- •8) Others, patients who are judged to be unacceptable as subjects of this study by the investigator or shared medical doctor
研究者
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