EUCTR2015-000290-12-ES进行中（未招募）1 期
Randomized Clinical Trial comparing the endometrial transformation with 25 mg/day of subcutaneous progesterone (Prolutex) versus 50 mg/day intramuscular progesterone (Prontogest)
Clínica IVI Barcelona0 个研究点开始时间: 2015年4月14日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Female age between 18 and 34 years (inclusive)
- •BMI between 18 and 28 kg / m2 (inclusive)
- •Endometrial thickness greater 7 mm on day of beginning progesterone treatment (day of follicular puncture)
- •Follicular maturation with bolus GnRH agonist
- •Egg donors who make a cycle of ovarian stimulation in the IVI Barcelona Centre
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 24
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known allergy to progesterone preparations or its excipients
- •Known allergy to estrogens
- •Known thrombophilia
- •Dependence on alcohol, drugs or psychotropic
- •Concurrent participation in another study
- •Concomitant medications that may interfere with the study medication and ovarian stimulation
- •Not complying the requirements for egg donors according to Law 14/2006 of 26 May 2006 on Assisted Human Reproduction Techniques
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