IRCT20080929001281N3已完成3 期
A randomized clinical trial to compare the effectiveness of oral contraceptives containing levonorgestrel, desogestrel, cyproterone acetate, and drospirenone on levels of adipokines, and adiposity indices in women with polycystic ovary syndrome.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 80
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 45 years（—）
- 性别
- Female
入选标准
- •Existence of diagnostic criteria for polycystic ovary syndrome based on Androgen Excess and PCOS Society (AES)
- •Age range: 18 to 45 years
排除标准
- •Use of hormonal; anti-androgen or insulin sensitizer drugs for at least 3 months before the study
- •Detection of severe hypertension; chronic disease; recent surgery or diagnosis of cancer
- •Appearing the serious side effects such as thrombosis
研究者
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