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临床试验/IRCT20090801002266N9
IRCT20090801002266N9招募中3 期

Efficacy of Bupropion on sexual function of women with orgasmic disorder

Esfahan University of Medical Sciences0 个研究点目标入组 30 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
30

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 50 years(—)
性别
Female

入选标准

  • Reading and writing literacy
  • Woman aged 18 to 50 years
  • Negative pregnancy test and no action for pregnancy during the intervention
  • Having a sexual partner (husband) who has no sexual dysfunction (spouse sexual intercourse is rejected by clinical interview).
  • She is in a marital relationship for at least six months, not considering divorce or separation, and alternately having sex with her husband.
  • The lack of active psychiatric illness Not having sexual desire and pain disorder (disparonius and vaginismus) simultaneously
  • Non-menopause (natural or surgical)
  • Not having a history of primary and secondary infertility The complaint of a global female orgasmic disorder should be as follows: a) Frequency of orgasms during sexual intercourse in less than 50% of sexual relationships. b) There is a disorder for at least 6 months. c) Has reached orgasm at least 3 times in the last 6 months.
  • Not having anxiety disorder at the same time (Beck anxiety disorder score less than 10).
  • Not having depressive disorder at the same time (Beck Depression Questionnaire score is less than 10).
  • Not having sexual and paraphilia disorders
  • History of seizure or head injury
  • No substance abuse or alcohol abuse over the past year
  • Non-use of psychiatric drugs and any drugs that affect sexual function (chronic use of opioids beta blockers, alpha-adrenergic drugs, psychotropic drugs)
  • Failure to receive synchronous psychological intervention

排除标准

  • Dissatisfaction to continue participating in the study at any time
  • Pregnancy during the study
  • Couple's death or divorce during the study

研究者

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