NCT01430650已完成4 期
A Randomised Control Trial to Evaluate Efficacy and Safety of Two Different Protocols of Endometrial Priming for Embryo Transfer.
Parc de Salut Mar1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2010年7月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 140
- 试验地点
- 1
- 主要终点
- Difference between day means in endometrial priming to achieve 7 mm.
研究概览
简要总结
The aim of this trial is compare two different endometrial priming protocols
- women that receive oral estrogens
- women that receive transdermal estrogens
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women between 18-50 years old with desire of children and needs of embryo transfer.
- •Plasma prolactin less than
- •Uterine cavity that allow pregnancy, body mass index between 20-
- •And signed consent inform.
排除标准
- •History of estrogen dependent cancer, unknown origin vaginal bleeding.
- •Ovarian cyst.
- •Contraindications to be pregnant.
- •Estrogen allergy.
研究组 & 干预措施
Oral strogen
Experimental
干预措施: Oral strogen (Drug)
Transdermal strogen
Experimental
干预措施: Transdermal strogen (Drug)
结局指标
主要结局
Difference between day means in endometrial priming to achieve 7 mm.
时间窗: 11-16 days
次要结局
- Biochemical Pregnancy rate(26-30 days)
- The patient's adherence to the recommended treatment.(1-16 days)
研究者
Miguel Angel Checa
MD
Parc de Salut Mar
研究点 (1)
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