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临床试验/IRCT20201216049736N1
IRCT20201216049736N1招募中3 期

Clinical trial comparing the efficacy and safety of N-acetylcysteine and amantadine on fatigue and disability and quality of life of patients with MS

Vice Chancellor for Research and Technology, Ahvaz Jundishapur University of Medical Sciences0 个研究点目标入组 112 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
112

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 50 years(—)
性别
All

入选标准

  • Patients with definitive diagnosis of MS aged 18 to 50 years
  • Be in the offensive phase (at least one month after the attack)
  • Disability rate according to EDSS criteria is between 1 to 5.5.
  • Fatigue is 4 or higher according to the FSS criteria.
  • If interferon is used to treat multiple sclerosis, at least 6 months have passed since the start of this drug.

排除标准

  • History of corticosteroid use during the month before treatment
  • Taking supplements or drugs with antioxidant properties such as vitamins E and C, zinc, melatonin
  • Taking medications that cause fatigue and drowsiness (such as benzodiazepines, tricyclic antidepressants,sedatives, anticonvulsants)
  • Taking stimulant drugs, amantadine, dopaminergic drugs
  • Pregnancy and lactation
  • History of NAC allergy or any side effects
  • Existence of depression (according to Beck questionnaire)
  • Accompanying medical conditions that can cause fatigue, such as: sleep disorders, heart failure, anemia, hypothyroidism and ....

研究者

发起方
Vice Chancellor for Research and Technology, Ahvaz Jundishapur University of Medical Sciences

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