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临床试验/NL-OMON31192
NL-OMON31192尚未招募不适用

A placebo-controlled, double blind study on the effect of a dopamine antagonist (Haloperidol??) on appetitive sexual conditioning in healthy female volunteers - Dopamine and classical conditioning of sexual responses

eids Universitair Medisch Centrum0 个研究点目标入组 128 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
128

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • female, heterosexual, no sexual complaints for at least one year, and sexually active including intercourse

排除标准

  • - Age < 18 or > 45 years
  • - BMI < 19
  • - Homosexual orientation (because of the *male* neutral stimuli)
  • - Pregnancy or lactation
  • - A diagnosis of affective, psychotic or substance related disorder according to DSM-IV-TR
  • - Having undergone a hysterectomy or prolapse surgery
  • - Using medication that may affect sexual response. To determine possible sexual side-effects the *Farmacotherapeutisch kompas* 2007 will be used.
  • - Current use of psycho-pharmacological medication, or recent use (less than 4 weeks before participation) of such medication
  • - Disorders of the genitals that may influence the sexual response or the measurement of the response
  • - Using drugs or medication that may interfere with haloperidol (for example alcohol, or medication that influences the central nervous system).
  • - A medical, and/or psychiatric illness or disorder, or a medical, and/or psychiatric history that indicates a risk in using haloperidol (for example cardiac arrhythmia, parkinson, depression, epilepsy, thyroid disorders).
  • - Use of alcohol or drugs 24 hours preceding participation in the experimental session

研究者

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