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临床试验/JPRN-jRCTs031180436
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

发起方
Watanabe Kota

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Efficacy of NAC for intervertebral disc degeneration. | 临床试验