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临床试验/TCTR20180523004
TCTR20180523004尚未招募3 期

A Randomized Controlled Trial of Thai Herbal Prasaplai Formula for Primary Dysmenorrhea: Extend study

Mahidol University0 个研究点目标入组 88 人开始时间: 2018年5月23日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
88

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 45 Years(—)
性别
Female

入选标准

  • Women aged 18-45 years.
  • The menstrution cycle duration is 21 to 35 days.
  • Diagnosed with primary dysmenorrhea.
  • Pain scores higher than or equal 4 out of 10 on Numeric Rating Scores (NRS) lasting for 3 months.

排除标准

  • History of allergy to ingredients contained in Plasaplai, starch and mefenamic.
  • Any gynecologic conditions confirmed of other pelvic pathologies by pelvic ultrasonography.
  • Placement of intrauterine devices or taking hormone.
  • History of abdominal surgery or other medical history which cause abdominal pain.
  • Using of any kind of analgesic drugs, medications or supplementary medicines.
  • Brest feeding, pregnant or likely to become pregnant within the next 6 months.
  • Blood transfusion within the last 3 months.
  • Smoking, alcoholism, or drug abuse.
  • Abnormal liver and renal functions.

研究者

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