跳至主要内容
临床试验/NL-OMON34740
NL-OMON34740已完成2 期

A double blind, randomized, cross-over placebo controlled study to investigate the efficacy of sublingual testosterone solution on physiological and subjective arousal in healthy, sexually dysfunctional premenopausal women. - PD-Testosterone

Emotional Brain0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
16

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

  • 1. Provision of written informed consent;
  • 2. Female 21-40 years of age with Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunctions e.g Female Sexual Arousal Disorder (FSAD) is allowed).
  • 3. Healthy according to normal results of medical history, physical examination, laboratory values and vital signs, unless the investigator considers an abnormality to be clinically relevant;
  • 4. Subject must be heterosexually oriented;
  • 5. BMI >= 18 and <= 30 kg/m2.

排除标准

  • 1. A history of Childhood Sexual Abuse;
  • 2. Subjects who had used testosterone therapy within 6 months before study entry;
  • 3. Use of oral contraception containing anti-androgens (e.g. Diane 35; Minerva);
  • 4. Use of oral contraception containing 50 µg estrogen or more;
  • 5. Pregnancy, or intention to become pregnant during this study (Note: a serum or urine pregnancy test will be performed in all women prior to the administration of study medications);
  • 6. Lactating, or subjects who have given birth in the previous 6 months;
  • 7. Subjects who are taking CYP3A4-inhibitors: ritonavir (HIV-proteaseremmer), ketoconazol en itraconazol claritromycine, erytromycine and saquinavir;
  • 8. Subjects who are taking CYP3A4-inducers: carbamazepine, fenytoïne, fenobarbital, st Johns Wort, rifampicine;
  • 9. A substance abuse disorder that in the opinion of the investigator is likely to affect the subject's ability to complete the study or precludes the subject*s participation in the study; mild or moderately alcohol drinking behavior is allowed, only 24 hours before the experimental days is alcohol drinking not allowed. Three weeks before the start of the experimental day is the taking of any recreational drug not allowed. Smoking is allowed.
  • 10. Subjects with a peri menopausal hormonal status (FSH > 30).

研究者

相似试验

进行中(未招募)
不适用
A double blind, randomized, cross-over placebo controlled study to investigate the efficacy of sublingual testosterone solution on physiological and subjective arousal in healthy, sexually dysfunctional premenopausal women. - PD testosterone
EUCTR2010-019540-39-NLEmotional Brain
进行中(未招募)
不适用
A double blind, randomized, cross-over placebo controlled study to investigate the subjective and physiological efficacy and safety of Lybrido and Lybridos in the domestic setting in healthy female subjects with Female Sexual Dysfunction in combination with SSRI use. - Lybrido(s) and SSRIs@HomeHypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunctions e.g Female Sexual Arousal Disorder (FSAD) is allowed) and/or SSRI induced sexual dysfunctioning.
EUCTR2009-016790-15-NLEmotional Brain
进行中(未招募)
不适用
A class-room experiment to investigate the genetic differences regarding effects of metoprolol in human volunteersInfluence of CYP2D6 polymorphism on metoprolol pharmacokinetics and pharmacodynamics in human volunteersMedDRA version: 18.0Level: HLGTClassification code 10007521Term: Cardiac arrhythmiasSystem Organ Class: 10007541 - Cardiac disordersMedDRA version: 18.0Level: PTClassification code 10015488Term: Essential hypertensionSystem Organ Class: 10047065 - Vascular disorders
EUCTR2015-002265-36-NLCentre for Human Drug Research
招募中
4 期
A randomized, double blind, crossover, placebo controlled class-room experiment to assess the pharmacodynamics and pharmacokinetics of metoprolol in healthy volunteers with different polymorphism of CYP2D6CYP2D6 polymorphism10082206
NL-OMON42822Centre for Human Drug Research50
进行中(未招募)
不适用
A double-blind, randomized, cross-over, placebocontrolled, 2-part study to compare the effect of exercise and high-dose salbutamol on maximal heart-rate in patients with COPD following therapeutic doses of inhaled QAB149 and salmeterol - NDCOPDMedDRA version: 6.1Level: PTClassification code 10009026
EUCTR2007-001051-19-ITOVARTIS FARMA24