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临床试验/IRCT20200617047808N1
IRCT20200617047808N1已完成1 期

Effects of oral Shilajit tablet on sexual function and sexual quality of life among married women of reproductive age: A triple blind; randomized; controlled; clinical trial study

Shahid Beheshti University of Medical Sciences0 个研究点目标入组 48 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
48

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 45-18 years
  • Iranian and living in Tehran
  • Literacy in Persian
  • Husband monogamy and living with the spouse now and during the study
  • Having sex in the last two months(According to the research unit)
  • No known underlying disease (diabetes, hypertension, asthma, heart disease, thyroid, pelvic visceral prolapse, tumor, other medical diseases, hyperlipidemia ...)
  • Do not have mental illness(According to the research unit or file)
  • Couples not addicted to drugs and alcohol(According to the research unit or file)
  • Do not use drugs that affect sexual function in the questionnaire (according to the research unit or file)
  • Have not had a stressful accident in the past month (according to the research unit)
  • Do not have a urinary tract infection (according to a recent research unit or test)
  • No vaginitis, cervicitis, pelvic genital pain disorders, active wound or genital lesion that interferes with sexual intercourse (penetration) (according to the examination and according to the statement of the research unit or file)
  • Has no history of being a rape victim (according to the research unit)
  • Has no history of infertility (according to the research unit)
  • No history of pelvic surgery (colpuraphy or correction according to the research unit or file)
  • Not sensitive to shellac or its compounds (according to the research unit)
  • Not pregnant or breastfeeding (according to the research unit)

排除标准

  • Not wanting to stay in the study
  • Do not take Shilajet tablets regularly (use less than 80% of cases)
  • Sensitivity to Shilajet pills or side effects during the study (according to the research unit)
  • Creating an active wound or lesion in the genital area that interferes with sexual intercourse (penetration) during the intervention (according to the research unit)
  • Consumption of drugs affecting sexual function during the intervention (according to the research unit)
  • Experience of a stressful incident during the intervention (according to the research unit)
  • Urinary tract infection, vaginitis, cervicitis, pelvic genital pain disorders, sexual abuse during the intervention (according to the research unit)
  • Pregnancy during the intervention (according to the research unit or a positive pregnancy test)

研究者

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