NL-OMON21403招募中不适用
PK-PD Testosterone: An investigator blind, randomized, cross-over placebo controlled dose finding study to investigate the pharmacokinetic profile of 3 doses of sublingual testosterone solution and their effect on physiological and subjective arousal in healthy, sexually functional premenopausal women.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 16
研究概览
简要总结
/A
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Provision of written informed consent;
- •2. Female 21-40 years of age;
排除标准
- •1. Sexual dysfunction as determined by Sexual Function Questionnaire (SFQ) diagnostic scores (within ‘high probability of dysfunction’ or ‘possibility of dysfunction’ ranges) for all functional domains (desire, arousal-lubrication, arousal-sensation, orgasm and pain) as described by Quirk et al. 2005;
- •2. Subjects who had used testosterone therapy within 6 months before study entry;
研究者
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