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临床试验/IRCT201402043706N21
IRCT201402043706N21已完成未知

Effect of combined calcium-vitamin D and only calcium on pain severity and menstrual bleeding in students with primary dysmenorrhea: a randomized placebo-controlled trial

Research deputy of Tabriz 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
未知
状态
已完成
发起方
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 30 years(—)
性别
Female

入选标准

  • painful and regular (35-21 days cycles) menstrual cycles during previous 3 months with maximum pain severity score of 5.0 to 9.1 assessed by VAS (0-10).
  • Having pain with features of primary dysmenorrhea (constant lower abdominal pain, radiating to the back or the anterior or medial thigh, starting several hours before or just after the menstrual flow).
  • No Known chronic disease (including epilepsy, gastrointestinal, cardio-vascular or renal diseases).
  • Being single.
  • Exclusion criteria:
  • No access to a phone line (for follow-up).
  • Occurrence of any type of genital diseases or abdominal or pelvic surgery in the last 6 months.
  • Experiencing any severe psychological stress, such as parental divorce, death of first degree relatives, etc. in the last 6 months.
  • Experiencing heavy vaginal bleeding (using a pad every hour for at least 6 hours) or continuous spotting between menstrual periods is in the last 6 months.
  • Having allergy to non-steroidal anti-inflammatory drugs.
  • Frequent and regular intake of supplements (including calcium, vitamin D, zinc, iron) in the last 3 months.

排除标准

  • 未提供

研究者

发起方
Research deputy of Tabriz university of medical sciences

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