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临床试验/IRCT2015062922982N1
IRCT2015062922982N1已完成2 期

The comparison of Zinc acetate and placebo (Avicil PH110) effects on primary dysmenorrhea

Vice Chancellor for Research, Islamic Azad Univercity, Falavarjan Branch0 个研究点目标入组 78 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
78

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 25 years(—)
性别
Female

入选标准

  • Single18 to25 years old students, intensity of pain was4 and more by visual analogue scale (VAS) , normal cycle (duration of cycle21-35 , bleeding3-7 days) , no history of abdominal or pelvic surgery or any specific disease such as hepatic, renal and cardiac diseases, diabetes, presence of secondary dysmenorrhea, non consumption of oral contraceptive pills in two months ago, no stressful condition in3 months ago and during the study like death of family members.
  • Exclusion criteria: Improper administration of the medication, administration of contraceptive pills or another medication whilst on research, severe stress, not to consent to continue the study.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research, Islamic Azad Univercity, Falavarjan Branch

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