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临床试验/NCT04748874
NCT04748874进行中(未招募)不适用

Immediate Versus Postponed Single Blastocyst Transfer in Modified Natural Cycle Frozen Embryo Transfer (mNC-FET): a Multicenter Randomized Controlled Trial

Rigshospitalet, Denmark2 个研究点 分布在 1 个国家目标入组 464 人开始时间: 2021年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
464
试验地点
2
主要终点
Live birth rate per randomized patient

研究概览

简要总结

The purpose of this randomized controlled trial is to investigate if immediate single blastocyst transfer (in the first menstrual cycle following oocyte retrieval) is non-inferior to standard postponed single blastocyst transfer (in the second or subsequent menstrual cycle following oocyte retrieval) in modified natural cycle frozen-thawed embryo transfer (mNC-FET) in terms of live birth rate.

详细描述

The study is a multicenter randomized non-blinded controlled trial with the purpose of investigating if immediate mNC-FET is non-inferior to standard postponed mNC-FET in terms of live birth rate and other obstetric- and neonatal outcome.

Several fertility clinics in Denmark will participate in the recruitment of patients. All clinics perform standardized treatments according to the public health care system in Denmark. Patient enrolment is expected to begin in February 2021 and continue until December 2024.

The study population will consist of 464 patients undergoing mNC-FET after a fresh IVF/ICSI cycle that did not result in a viable pregnancy, or after a freeze-all cycle. Eligible patients will be recruited if they fulfil the inclusion criteria and none of the exclusion criteria. Patients will be randomized 1:1 by simple randomization to one of the following study arms:

I. Immediate mNC-FET In the Immediate arm, patients will undergo mNC-FET in the menstrual cycle immediately following oocyte retrieval with failed fresh embryo transfer or freeze-all.

II. Postponed mNC-FET In the Postponed arm, mNC-FET is performed at least one full menstrual cycle after the fresh embryo transfer or freeze-all cycle, which means that the first FET following the fresh cycle is not started until the second menstrual bleeding or later.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients eligible for FET in a modified natural cycle
  • Regular menstrual cycle (23-35 days)
  • Vitrified day 5 or 6 blastocyst
  • Blastocyst Gardner score > or = 3BB at the day of vitrification

排除标准

  • Uterine malformations or presence of hydrosalpinx
  • Submucosal uterine myomas
  • Uterine polyps
  • Allergy to standard fertility medication
  • Contradiction to standard fertility medication
  • Male of female HIV, hepatitis B or C
  • Preimplantation Genetic Testing (PGT) in the fresh cycle
  • Severe OHSS during the fresh cycle (defined as need for ascites drainage and/or hospital admission)
  • Oocyte donation
  • Testicular sperm aspiration (TESA)

结局指标

主要结局

Live birth rate per randomized patient

时间窗: One-year follow-up after a positive pregnancy test

Live birth rate in patients randomized to immediate versus postponed FET

Live birth rate per protocol

时间窗: One-year follow-up after a positive pregnancy test

Live birth rate in patients randomized to immediate versus postponed FET minus dropouts

次要结局

  • Positive hCG rate per randomized patient and per blastocyst transfer(16 days after ovulation trigger (hCG+16))
  • Ongoing pregnancy rate per randomized patient and per blastocyst transfer(Ultrasound at 7-8 weeks of gestation)
  • Day of ovulation(From first day of FET cycle to the day of ovulation trigger (hCG+0), up to 1 month)
  • Neonatal outcome(One-year follow-up after a positive pregnancy test)
  • Clinical pregnancy loss(Routine ultrasound at 7-8 weeks of gestation or ad hoc ultrasound before 22 weeks of gestation)
  • Cycle cancellation(16 days after ovulation trigger (hCG+16) and through study completion, up to 1 year)
  • Reason for cycle cancellation(16 days after ovulation trigger (hCG+16) and through study completion, up to 1 year)
  • Pregnancy related complications(One-year follow-up after a positive pregnancy test)
  • Time-to-live-birth(From day of ovarian stimulation through study completion, up to 18 months)
  • Live birth rate per blastocyst transfer(One-year follow-up after a positive pregnancy test)
  • Biochemical pregnancy loss(16 days after ovulation trigger (hCG+16) and up to 7-8 weeks)
  • Number of ovarian follicular structures >10 mm(At baseline and on day of ovulation trigger (hCG+0), up to 1 month)
  • Time-to-pregnancy(From day of ovarian stimulation to day of clinical pregnancy, up to 1 year)
  • Quality of life assessment(Baseline and mid-luteal phase (hCG+11), up to 1 month)
  • Endocrinology of the luteal phase(Baseline, day of ovulation trigger (hCG+0), early luteal phase* (hCG+4), day of transfer (hCG+6) and mid-luteal phase* (hCG+11)(*only at Rigshospitalet), within one FET cycle, up to approximately 1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kristine Loessl

MD, PhD

Rigshospitalet, Denmark

研究点 (2)

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