跳至主要内容
临床试验/CTIS2024-515811-22-00
CTIS2024-515811-22-00进行中(未招募)1 期

Exploratory study on the impact of different doses and route of administration of exogenous progesterone in artificial endometrial preparation cycles on endometrial structure and function - 1901-VLC-014-E

Ivi Valencia S.L.0 个研究点目标入组 108 人开始时间: 2024年6月26日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
108

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 至 64(—)

入选标准

  • All women with no history of infertility who agree to participate in the study: 1. Informed consent form (ICF) dated and signed. 2. Age: 18-35 years old , both inclusive 3. Regular menstrual cycles (between 22 and 35 days) 4. In good health and not suffering from any mental or medical condition(s) that would preclude participation in the study

排除标准

  • Subjects who meet one or more of the following will not be considered eligible to participate in the pilot study: 1.Simultaneous participation in other clinical studies that, at the researcher's criteria, could interfere with the results of this study. 2.Taking contraceptives in the three months prior to signing informed consent. 3.Presence of uterine pathology (submucosal or intramural myomas >4 cm deforming cavity, endometrial polyps or müllerian anomalies) or adnexal pathology (communicating hydrosalpinx). 4.Background of thrombosis, breast cancer, systemic diseases. 5.Those unable to comprehend the investigational nature of the proposed study.

研究者

发起方
Ivi Valencia S.L.

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