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临床试验/DRKS00022943
DRKS00022943已完成不适用

Prospective Observational Post-Authorisation Study on Fresh-transfer and Freeze-all treatments of ART patients undergoing controlled ovarian stimulation with Follitropin alfa (Bemfola®) - FREEZE-A

GEDEON RICHTER PHARMA GmbH0 个研究点目标入组 956 人开始时间: 2020年8月24日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
956

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
Female

入选标准

  • Eligible patients must meet the following criteria:
  • - Adult female patient with an indication for IVF/ICSI treatment
  • - Planned first ART stimulation cycle
  • - Planned to receive Bemfola® as monotherapy for ovarian stimulation
  • - Signed Informed Patient Consent form (ICF)

排除标准

  • Eligible patients must not meet the following criteria:
  • - History of previous poor response to gonadotropins outside ART
  • - Planned Fertility Protection (due to malignancies etc.)
  • - Ovarian Random Start and Duo Stimulations
  • - Serum AMH-Level < 1,0 ng/ml

研究者

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