EUCTR2014-004784-20-ES进行中（未招募）不适用
Subcutaneous progesterone ( Prolutex ) versus vaginal progesterone capsules (Progeffik) for endometrial preparation in fresh donated oocyte recipients: A prospective, randomized, single-blind, pilot trial.
Instituto Bernabeu0 个研究点开始时间: 2014年12月16日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 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 49 years (inclusive)
- •Women who want pregnancy
- •Endometrial thickness greater than 7 mm on the randomization of the patient is made to a group of progesterone
- •more than 6 oocytes retrieved from the donor woman
- •Patient scheduled for fresh embryo transfer on day +5 embryo culture
- •BMI greater than 30 kg / m2
- •Infertility justify treatment with donor oocytes Women
- •Males no known alterations in karyotype
- •Semen ejaculation from either the partner or from bank
- •Uterus able to support embryo implantation and pregnancy
- •Absence of pregnancy before starting the cycle of embryo transfer
- •Have consented in writing
- •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 120
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Important endocrine-metabolic Systemic diseases affecting pituitary, thyroid, adrenals, pancreas, liver or kidney
- •Seropositivity for HIV, HBV or HCV
- •Undiagnosed vaginal bleeding
- •Pregnancy, lactation or contraindication for pregnancy
- •Malformations of sexual organs incompatible with pregnancy
- •Known allergy to preparations of progesterone or its excipients
- •Current dependence on alcohol, drugs or psychotropic
- •Concurrent participation in another study
- •Concomitant medication that could interfere with study medication
研究者
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