Impact of luteal phase support with vaginal progesterone on the clinical pregnancy rate in IUI cycles stimulated with gonadotrophins: a prospective randomized multicentre study. - Luteal Phase and IUI

niversity Hospital Leuven0 个研究点目标入组 393 人开始时间: 2011年2月1日最近更新: 2021年3月30日

试验速览

暂无简介。

•Women: Normo-ovulatory ( cycles: 26-32d), age<43, BMI=30. Presence of at least one patent tube on hysterosalpingography and/or laparoscopy, normal uterine cavity (ultrasound, hysterosalpingography, or laparoscopy)
•Men: Sperm sample with a total motile count = 5 Miljon/ml after capacitation
•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
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range

•Patients with a contra indication for the use of crinone :
•Known hypersensitivity to progesterone or one of the components of Crinone, vaginal bleeding of unknown origin, known or suspected malignancy of the breast or the reproductive system, acute porphyria, meningioma, patients with a history of or experiencing thrombophlebitis, trombo-embolic disease or cerebrovascular accident, non-ongoing pregnancy

发起方

niversity Hospital Leuven