ACTRN12608000429358进行中（未招募）2 期
A Phase II open-label pilot study to assess the effects of Testosterone Metered Dose Transdermal System (MDTS) administration on cognitive function in women
FemPharm Pty Ltd0 个研究点目标入组 10 人开始时间: 2008年8月26日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 45 Years 至 60 Years（—）
- 性别
- Female
入选标准
- •Healthy postmenopausal women on stable non-oral oestrogen for at least 8 weeks
排除标准
- •history of cancer exluding non-melanotic skin cancer, significant heart, liver, kidney, endocrine disease or neurological disease, androgenic alopecia, current androgen or anti-androgen therapy, epilepsy, seizures, psychiatric illness, previous neurological or head injury, intellectual disability, uncontrolled hypertension, recent major gynaecological surgery, total tesosterone levels higher than the upper limit of the normal reference range for young premenopausal women, alcohol consumption of greater than 3 standard drinks per day, if uterus in situ use of progestin other than Mirena intra-uterine device, presence of implanted metallic material or devices, severe claustrophobia
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