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临床试验/IRCT20190430043433N1
IRCT20190430043433N1招募中3 期

Compare the effect of acupressure therapy and Fluoxetine on the symptoms of premenstrual syndrome: A randomized clinical trial

Qazvin University of Medical Sciences0 个研究点目标入组 90 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
入组人数
90

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 35 years(—)
性别
Female

入选标准

  • The desire to participate in the study
  • Regular menstruation from 24 to 35 days
  • The normalization of the length and volume of menstrual bleeding is 3-10 days
  • Age range 18 to 35 years
  • Having a Body Mass (25 -5/18)
  • . Having symptoms of premenstrual syndrome in two cycles before starting the intervention
  • Non-Depression Based on the Beck Questionnaire
  • Having a phone number to follow

排除标准

  • Having known psychological illnesses (according to the person)
  • Use of any drug for the treatment of premenstrual syndrome
  • Tobacco use, narcotics and psychotropic drugs (according to the person)
  • Having regular exercise
  • Use of antidepressants, sedation and hormones and vitamin supplements
  • There are skin lesions in acupressure points
  • A stressful incident in the past six months, such as: separation of parents, death of first-degree family members, and ....
  • Use of any drug that has fluoxetine interactions

研究者

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