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临床试验/NCT07818278
NCT07818278尚未招募4 期

Cycle-to-cycle Variability of Progesterone in the Endometrium in Patients Undergoing an Euploid Blastocyst Transfer in a Hormone Replacement Therapy (HRT) Cycle (PROMICOFET)

University Hospital, Ghent1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2026年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
尚未招募
入组人数
70
试验地点
1
主要终点
Endometrial hormonal concentrations

研究概览

简要总结

This study looks at progesterone, a hormone that prepares the womb lining (endometrium) for pregnancy, in women having a frozen embryo transfer after IVF. Before an embryo is transferred, women take estrogen and progesterone medication to prepare the endometrium. Doctors currently check progesterone levels in the blood, but blood levels do not always match what is happening in the endometrium itself, and it is not yet known whether progesterone levels in the womb tissue stay the same from one treatment cycle to the next.

The study also looks at whether hormone levels relate to how the uterus contracts, to the bacteria naturally present in the vagina, cervix, uterus and gut, and to tiny particles released by cells (called extracellular vesicles) that may help the embryo and the womb "communicate" during implantation.

Participants are women who are already waiting for genetic test results on their embryos, a wait that typically lasts around 8 weeks. During this time, they go through two practice ("mock") treatment cycles using the same hormone medications as a real embryo transfer, but without an actual embryo. During these cycles, researchers collect blood and urine samples, a small tissue sample from the womb lining, swabs from the vagina, cervix and rectum, and a short ultrasound recording of womb movement. Afterwards, participants proceed with their real embryo transfer cycle, with similar (though fewer) measurements taken, and are followed to see whether they become pregnant.

The findings from this study may help doctors better understand how to personalize hormone treatment for future frozen embryo transfers, with the aim of improving pregnancy outcomes.

详细描述

This is a prospective, single-center pilot study conducted at the Department of Reproductive Medicine, Ghent University Hospital, in women undergoing preimplantation genetic testing for aneuploidy (PGT-A) prior to euploid blastocyst transfer in a hormone replacement therapy (HRT)-prepared frozen embryo transfer (FET) cycle. The pilot design was chosen because data on the interaction between endometrial and serum hormonal levels, the reproductive tract and fecal microbiome, uterine peristalsis, and embryo- and maternal-derived extracellular vesicles (EVs) in this setting are currently limited.

Each subject undergoes two mock HRT cycles during the approximately 8-week PGT-A waiting period, followed by one embryo transfer cycle. Endometrial preparation in each cycle consists of transdermal estradiol gel (Oestrogel®) until adequate endometrial thickness is reached, followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day) for 6.5 days. In the mock cycles, no embryo is transferred; instead, study-specific procedures are performed, including endometrial biopsy for tissue hormonal quantification by UPLC-MS/MS, a mock embryo transfer with catheter tip collection for endometrial microbiome analysis, transvaginal ultrasound with speckle-tracking analysis of the uterine junctional zone to characterize contraction frequency, amplitude, and velocity before, during and after the procedure, and collection of vaginal, cervical and rectal swabs, urine, and blood for hormonal and extracellular vesicle profiling. The embryo transfer cycle follows the same sampling scheme (excluding endometrial biopsy) around an actual euploid blastocyst transfer performed under standard of care. Follicular fluid at oocyte pick-up and embryo culture media (collected on days 3 and 6 of embryo culture) are additionally retained for extracellular vesicle analysis, material that would otherwise be discarded during routine IVF laboratory processing.

Beyond the primary focus on intercycle reproducibility of endometrial tissue progesterone, the study explores associations between hormonal levels, uterine contractility, reproductive-tract and fecal microbiome composition, and extracellular vesicle cargo, with the broader aim of identifying candidate biomarkers of endometrial receptivity to inform future optimization of luteal phase support.

Given the established safety profile of the authorized study medications (Utrogestan® and Oestrogel®), adverse event and serious adverse event collection is selective, focused on events not attributable to standard-of-care fertility procedures; a Data Safety Monitoring Board was not deemed necessary.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
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

  • Age ≥18 and ≤40 years old.
  • BMI ≥ 18 kg/m² and < 35 kg/m².
  • Current pregnancy wish.
  • PGT-A tested patients, undergoing a euploid blastocyst transfer in an artificial cycle.
  • Dutch, French and/or English speakers, as informed consent forms (ICFs) are made in those three languages.

排除标准

  • Known reasons for impaired implantation (specifically: presence of a hydrosalpinx; presence of a type I, II or III fibroid; Asherman's syndrome; uterine malformations; intrauterine adhesions; ≥ grade 3 endometriosis according to the ASRM classification, endometrial tuberculosis, adenomyosis).
  • Abnormal (not menstrual) vaginal bleeding without a known/diagnosed cause.
  • Tumours of the ovary, breast, uterus, pituitary or hypothalamus.
  • Untreated and uncontrolled thyroid dysfunction.
  • Personal history of a thromboembolic event.
  • Use of carbamazepine, rifampicin, phenytoin.
  • Subjects unable to comprehend the investigational nature of the proposed study.
  • Patients with a history of known thin endometrium (< 5 mm).

研究组 & 干预措施

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Oestrogel® 0.75 mg (estradiol transdermal gel) (Drug)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Progesterone 200 mg vaginal capsules (Drug)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Endometrial biopsy (Procedure)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Mock embryo transfer (Procedure)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Transvaginal ultrasound with uterine peristalsis assessment (Procedure)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Biological sample collection (blood, urine, vaginal/cervical/rectal swabs, follicular fluid, embryo culture media) (Procedure)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Embryo transfer catheter tip collection for bacterial DNA analysis (Procedure)

HRT-Prepared FET with Endometrial and Biofluid Sampling

Experimental

All enrolled participants undergo HRT endometrial preparation - transdermal estradiol gel (Oestrogel®) followed by vaginal micronized progesterone (Utrogestan®, 800 mg/day for 6.5 days) - across three consecutive artificial cycles: two mock cycles and one embryo transfer cycle, conducted during the standard-of-care waiting period for PGT-A results.

In each mock cycle, participants undergo: endometrial biopsy, a mock embryo transfer (with catheter tip collection for microbiome analysis), transvaginal ultrasound (uterine peristalsis), and collection of vaginal, cervical and rectal swabs, urine, and blood samples for hormonal profiling and extracellular vesicle analysis.

In the embryo transfer cycle, an actual euploid blastocyst is transferred under standard clinical care, with the same non-invasive study-specific sampling performed (excluding endometrial biopsy). Participants are followed for pregnancy outcomes.

干预措施: Questionnaires and pain assessment (VAS) (Other)

结局指标

主要结局

Endometrial hormonal concentrations

时间窗: For an individual patient: mock embryo transfer cycles 1 and 2. Approximately 8 weeks. For the whole study: through the study completion, approximately 2 years since start of recruitment.

Endometrial biopsies will be taken in mock embryo transfer cycles 1 and 2, on the day of mock transfer (day 6 after progesterone administration). This tissue will be sent to the clinical biology department in the hospital UZ Gent, to perform UPLC-MS/MS and obtain the concentration of progesterone, estradiol, estrone, 17α-hydroxyprogesterone in the tissue. This will later be correlated with the other outcome measurements: hormonal levels in blood, microbiome composition, uterine peristalsis, EV composition, etc. The concentrations will be obtained in ng/ml or μg/ml.

次要结局

  • Hormonal levels in blood(From OPU (oocyte pick-up day) until pregnancy follow-up visit (between 6 and 8 weeks of gestation))
  • Microbiome composition(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Clinical pregnancy outcomes: biochemical pregnancy(Follow-up pregnancy visit (6-8 weeks of gestation))
  • Clinical pregnancy outcomes: live birth(Follow-up pregnancy (6-8 weeks of gestation) until live birth (up to approximately 40 weeks after embryo transfer))
  • Clinical pregnancy outcome: miscarriage(From the follow-up pregnancy (6-8 weeks of gestation) visit until miscarriage happens (before 22 completed weeks of gestational age).)
  • Clinical pregnancy outcome: clinical pregnancy(Follow-up pregnancy visit (6-8 weeks of gestation))
  • Questionnaire about lifestyle and dietary habits for better analysis of microbiome composition(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Visual Analogue Scale (VAS) for (mock) embryo transfer(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Uterine waves/peristalsis analysis - contraction coordination(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Uterine waves/peristalsis analysis - contraction velocity(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Uterine waves/peristalsis analysis - contraction direction(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Uterine waves/peristalsis analysis - contraction amplitude(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • Uterine waves/peristalsis analysis - contraction frequency(On the day of (mock) embryo transfer through the three identically prepared HRT cycles. Approximately 3 months per patient.)
  • EVs composition in blood, follicular fluid and urine (maternal), and embryo culture media(From OPU (oocyte pick-up day) until pregnancy follow-up (between 6 and 8 weeks of gestation))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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