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临床试验/NCT03998761
NCT03998761已完成不适用

Micronized Progesterone Versus Micronized Progesterone Plus Dydrogesterone for Luteal Phase Support in Frozen - Thawed Transfer: a Prospective Cohort Study

Mỹ Đức Hospital1 个研究点 分布在 1 个国家目标入组 1,364 人开始时间: 2019年6月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,364
试验地点
1
主要终点
Live birth rate

研究概览

简要总结

Frozen embryo transfer (FET) has been increasing important in IVF. Progesterone is essential for the endometrial secretory transformation, establishment and maintenance of pregnancy. In FET, as there is neither corpus luteum nor the support of hCG, the role of progesterone is even more important to ensure a sufficient luteal phase support.

Vaginal progesterone has been the most common preparation for luteal support in fresh embryo transfer during IVF because of their ease of use and comparable effectiveness compared to intramuscular progesterone. Recently, there was evidence of the considerable variation in uptake, absorption and metabolism of intra-vaginal micronized progesterone. Dydrogesterone alone has described to have similar effectiveness, safety and tolerability prolfiles for luteal phase support compared to vaginal progesterone in luteal phase support for fresh embryo transfer. This prospective study compares the effectiveness of micronized progesterone versus micronized progesterone plus dydrogesterone for luteal phase support in FET.

详细描述

All patients undergoing FET will receive oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day from the second or third day of menses for 6 days. Endometrial thickness will be monitored from day six onwards. From day 8-9 of menses, the estradiol dose could be adjusted from 8mg/day to 16mg/day according the development of the endometrium. Progesterone will be started when endometrial thickness reached 8 mm or more. In the first four months, all the patients will be treated with micronized progesterone. In five months later, the intervention will be changed to micronized progesterone plus dydrogesterone. In the second group of patients, the duration of study will be extended for one month due to the Lunar New Year holiday.

Group 1: Micronized progesterone Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening).

Group 2: Micronized progesterone plus dydrogesterone Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston 10mg) at the dose of 10mg twice daily (morning and evening).

In both group, on the day of starting progesterone, the dose of estradiol will be decreased to 8mg/day. A maximum of 2 embryos will be thawed on the day of embryo transfer, which is four days or six days after the start of progesterone depending on day-3 or day-5 embryo transfer. After thawing, surviving embryos will be transferred into the uterus under ultrasound guidance. Estradiol and progesterone will be continued until the day of pregnancy test. If the pregnancy test is positive, the patients will continue to use 800 mg micronized progesterone or 800 mg micronized progesterone plus 20 mg dydrogestetrone, until 7 weeks of gestation.

Blood samples will be obtained at day 4 after the use of progesterone. Serum progesterone will be measured. The blood tests will be taken in the morning, 2-3 h after the dydrogesterone and/or micronized progesterone application.

研究设计

研究类型
Interventional
分配方式
Non 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 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Undergoing frozen embryo transfer
  • Endometrial prepared by exogenous hormonal regimen
  • Permanent resident in Vietnam

排除标准

  • Having > 2 embryo transfer attempts
  • Having embryo(s) from donors cycles
  • Having embryo(s) from IVM
  • Having embryo(s) from PGT/PGS
  • Having endometrial abnormalities: polyp, sub-mucosal fibroid, cesarean scar defects, endometrial hyperplasia, endometrial fluid accumulation, endometrial adhesion.
  • Participating in another IVF study at the same time

研究组 & 干预措施

Micronized progesterone

Active Comparator

Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening).

干预措施: Micronized Progesterone (Drug)

Micronized progesterone plus dydrogesterone

Active Comparator

Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston® 10mg, Abbott) at the dose of 10mg twice daily (morning and evening).

干预措施: Micronized progesterone plus dydrogesterone (Drug)

结局指标

主要结局

Live birth rate

时间窗: At least 24 weeks of gestation up to the time of delivery

The birth of at least one newborn after 24 weeks of gestation that exhibits any sign of life such as respiration, heartbeat, umbilical pulsation or movement of voluntary muscles (twin will be a single count).

次要结局

  • The luteal progesterone level(On day four of the progesterone application)
  • Gestational diabetes rate(At 24 weeks of gestation)
  • Antepartum haemorrhage rate(From 24 weeks of gestation up to at birth)
  • Ectopic pregnancy rate(At 12 weeks of gestation)
  • Birth weight (grams) of singletons and twins(At birth)
  • Low birth weight rate(At birth)
  • Gastrointestinal disorders rate(At 7 weeks of gestation)
  • Vulvovaginal pruritus rate(At 7 weeks of gestation)
  • The length of luteal phase(On day sixteen of progesterone application)
  • Very high birth weight rate(At birth)
  • Venous thromboembolism (VTE) rate(At 7 weeks of gestation)
  • Positive pregnancy test rate(On day sixteen of progesterone application)
  • Ongoing pregnancy rate(At 12 weeks' gestation)
  • Miscarriage rate(At 12 weeks of gestation)
  • Multiple pregnancy rate(At 7 weeks' gestation)
  • Hypertensive disorder of pregnancy rate(From 20 weeks of gestation up to at birth)
  • High birth weight rate(At birth)
  • Clinical pregnancy rate(At 7 weeks of gestation)
  • Implantation rate rate(At 3 weeks after embryo transferred)
  • Preterm delivery rate(At birth)
  • Very low birth weight rate(At birth)
  • Congenital anomaly diagnosed at birth rate(At birth)
  • Nervous system disorders rate(At 7 weeks of gestation)
  • Vaginal discharge rate(At 7 weeks of gestation)
  • Vaginal discomfort rate(At 7 weeks of gestation)

研究者

发起方
Mỹ Đức Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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