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临床试验/2024-519126-20-00
2024-519126-20-00招募中4 期

Benefit of GnRH Agonist Before Frozen Embryo Transfer in Patients With Endometriosis and/or Adenomyosis: Randomised Prospective Study.

Hospital Foch1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2024年11月15日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
招募中
发起方
Hospital Foch
入组人数
180
试验地点
1
主要终点
The primary evaluation criterion is the clinical pregnancy rate (confirmed by the presence of a fetal heartbeat), which will be assessed in both groups during the ultrasound conducted at the final visit

研究概览

简要总结

To assess the impact of the administration of a long-acting GnRH agonist prior to frozen embryo transfer (FET) on clinical pregnancy rates within an assisted reproductive technology (ART) protocol, in patients with endometriosis and/or adenomyosis.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
性别
Female
接受健康志愿者

入选标准

  • Women aged 18 to 36 with endometriosis and/or adenomyosis
  • Having undergone IVF/ICSI with freeze-all, and for whom a blastocyst FET is planned
  • A normal uterine cavity
  • An MRI with contrast injection confirming endometriosis and/or adenomyosis during the inclusion visit (MRI performed after patient selection if no results from the past 6 months are available or interpretable)
  • Having signed a consent form
  • Affiliated with a health insurance plan

排除标准

  • Pregnancy and breast
  • History of implantation failures (≥2)
  • Endometrial abnormalities
  • Known uni or bilateral hydrosalpinx
  • Known hypersensitivity to GnRH, GnRH analogues, or any excipients in DECAPEPTYL® LP, 11.25 mg
  • Known hypersensitivity to estradiol/progesterone/acetylsalicylic acid/folic acid/cefixime/levofloxacin
  • Known or suspected breast cancer, or history of breast cancer
  • Known or suspected cancer of the reproductive system, or history of reproductive system cancer
  • Known or suspected estrogen-dependent malignant tumors

结局指标

主要结局

The primary evaluation criterion is the clinical pregnancy rate (confirmed by the presence of a fetal heartbeat), which will be assessed in both groups during the ultrasound conducted at the final visit

The primary evaluation criterion is the clinical pregnancy rate (confirmed by the presence of a fetal heartbeat), which will be assessed in both groups during the ultrasound conducted at the final visit

次要结局

  • Number of successful implantations per number of embryos transferred;
  • Miscarriage defined as a spontaneous pregnancy loss after a successful implantation;
  • Incidence and severity of side effects related to hypoestrogenism (e.g., hot flashes, night sweats, decreased libido, mood swings, etc.)

研究者

发起方
Hospital Foch
申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

PIRTEA Paul

Scientific

Hospital Foch

研究点 (1)

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