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临床试验/NCT07072052
NCT07072052尚未招募不适用

Oxford Luteal Dysfunction and Placental Insufficiency Study

University of Oxford1 个研究点 分布在 1 个国家目标入组 360 人开始时间: 2025年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
360
试验地点
1
主要终点
Correlation between early luteal secretory product levels and preeclampsia risk

研究概览

简要总结

High blood pressure (BP) affects approximately 1 in 10 pregnancies. About half of women with high blood pressure in pregnancy develop a serious complication called preeclampsia, which kills over 70,000 women and 500,000 babies every year worldwide. Despite its devastating impact, scientists know little about preeclampsia prevention or treatment. Research has shown that preeclampsia results mainly from an abnormal attachment of the placenta to the lining of the womb. In the first 8 weeks of pregnancy, placental attachment depends on the release of hormones (for example, progesterone) by a gland in the ovary called the corpus luteum. Low blood levels of progesterone in early pregnancy are associated with a reduced chance of having a live baby and higher risk of miscarriage. Giving progesterone to women at risk of miscarriage in early pregnancy reduces their chance of developing preeclampsia by nearly 40%. These results highlight the crucial role of the corpus luteum in normal pregnancy, but there is a need for high-quality studies to identify women whose corpus luteum may be defective. Giving these women medicines to treat corpus luteal defects may lead to normal attachment of the placenta, reducing the risk of pregnancy complications such as preeclampsia. The investigators propose a study that will investigate whether ultrasound features of the corpus luteum and blood and urine levels of corpus luteal hormones may predict preeclampsia.

详细描述

The corpus luteum (CL), formed in the ovary after ovulation, secretes a range of molecules (e.g., oestradiol, progesterone, vascular endothelial growth factor [VEGF], relaxin-2) that regulate embryo implantation and placentation.1 Without a CL, early pregnancy invariably fails, unless women receive exogenous hormone replacement.2 After 8 weeks of pregnancy, the placenta takes over endogenous hormone synthesis from the CL, ensuring pregnancy maintenance until birth; this is termed the luteo-placental shift.2 3 Placental maladaptation is the principal driver of preeclampsia, a pregnancy complication that kills >70,000 women and 500,000 babies annually worldwide.4 Despite its catastrophic effects, there remains a paucity of interventions to prevent or treat preeclampsia. The best tool currently available to predict preeclampsia in the index pregnancy is a validated algorithm which can only be used at 10-14 weeks (the Fetal Medicine Foundation [FMF] Preeclampsia prediction tool, whose positive predictive value is 90%).5

The role of the CL in orchestrating placentation has recently gained prominence following a huge rise in frozen embryo transfer (FET) treatment in assisted conception.6 There are different methods of preparing the endometrium for FET. These include unmedicated regimens, relying on the woman's menstrual cycle to time embryo transfer; and medicated protocols, involving the administration of oestradiol and progesterone before embryo transfer.7 The latter suppresses the pituitary gland, preventing ovulation and the formation of a CL. Uniquely, pregnancies resulting from medicated FET cycles are the only gestations capable of reaching viability without a CL, and are only able to progress because of early hormone replacement.8

Pregnancies without a functioning CL exhibit more than double the odds of preeclampsia (odds ratio [OR] 2.13, 95% confidence interval [CI] 1.89-2.38; 4 studies; n = 22,856 women) versus pregnancies with a functioning CL,8 highlighting a crucial role of the CL in preventing placental maladaptation. Our previous work has elucidated this role by showing a strong association between low luteal serum progesterone and reduced odds of live birth (adjusted OR 0.41, 95% CI 0.18-0.91).9 10 We have also demonstrated that administering exogenous progesterone in early pregnancy significantly reduces the incidence of preeclampsia (risk ratio [RR] 0.61, 95% CI 0.41-0.92; 3 randomised controlled trials [RCTs]; I2 = 0%; n = 5,267 women).11 These findings provide a strong signal that luteal phase insufficiency plays a fundamental role in placental maladaptation, yet crucially it appears amenable to exogenous rescue.

Case-control evidence suggests an association between low serum levels of corpus luteal products, including progesterone and relaxin-2, and the risk of preeclampsia, although data remain scarce and of low quality.12 13 In addition, current practice involves screening women in early pregnancy for their risk of preeclampsia based on their history, yielding a detection rate that is at most 30%.14 Identifying blood and ultrasound markers in early pregnancy associated with the risk of developing preeclampsia later on would allow to develop diagnostic tests and therapeutic targets to prevent preeclampsia.

Therefore, this study aims to establish the association between early serum and ultrasound markers of corpus luteal function and pregnant women's risk of developing preeclampsia. By focusing on recruiting women in very early gestation (<8 weeks), we aim to develop a set of prognostic markers which will help to better identify women at high risk of developing preeclampsia as early as possible. This will allow for better risk stratification in this population, and for future trials investigating interventions to prevent preeclampsia from early gestation rather than at 12 weeks (e.g., when aspirin is currently commenced) which may be too late to effectively correct placental maladaptation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Participant is willing and able to give written informed consent for participation in the study.
  • Female, aged 16 years or above. As in vitro fertilisation is not undertaken in women younger than 18 years, those with pregnancies resulting from natural cycle frozen embryo transfer will be aged 18 years or above.
  • Pregnancy <8 completed weeks of gestation (i.e., up to 7 weeks and 6 days' gestation).
  • Conception through any of the following means: unassisted ("natural"), ovulation induction (with clomifene citrate, letrozole or gonadotropin injections, including trigger injection), intrauterine insemination (with or without ovulation induction, including trigger injection), or natural cycle frozen embryo transfer.
  • Intrauterine viable pregnancy confirmed on research ultrasound scan.
  • Intention to deliver at Oxford University Hospitals.

排除标准

  • Unable to read, or to understand written or spoken English.
  • Vaginal bleeding at first visit.
  • Miscarriage at first visit, defined as fetal crown-rump length of 7 mm or longer with no visible heartbeat, OR gestational sac with a mean of 25 mm or greater in diameter with no visible fetal pole on ultrasonography.
  • Evidence of ectopic pregnancy at first visit.
  • Multiple pregnancy.
  • Uterine pathology (e.g., uterine polyp, fibroid, septate uterus, uterus didelphys, bicornuate uterus, unicornuate uterus).
  • Fresh in vitro fertilisation.
  • Donor oocyte in vitro fertilisation.
  • Frozen embryo transfer using hormone replacement therapy for endometrial preparation.
  • Participation in any concurrent trials of medicinal products in pregnancy.

结局指标

主要结局

Correlation between early luteal secretory product levels and preeclampsia risk

时间窗: Collected data and samples will be analysed blindly throughout the study and compared between the two main time points: <8 weeks' gestation (research visit 1) 10-14 weeks' gestation (research visit 2)

To evaluate the correlation between individual levels of corpus luteum secretory products at \<8 weeks' gestation: progesterone (ng/mL), oestradiol (pmol/mL), vascular endothelial growth factor (VEGF) and Relaxin-2, measured in serum/plasma and the predicted probability (%) of developing preeclampsia at 10-14 weeks' gestation using the validated Fetal Medicine Foundation Preeclampsia Prediction Algorithm.

Correlation between luteal ultrasound features and preeclampsia risk

时间窗: Collected data and samples will be analysed throughout the study and compared between the two main time points: <8 weeks' gestation (research visit 1) 10-14 weeks' gestation (research visit 2)

Evaluate the correlation between ultrasound imaging characteristics (corpus luteum size and vascularity index measured by power Doppler), and the calculated probability (%) of developing preeclampsia, as predicted by the Fetal Medicine Foundation Preeclampsia Prediction Algorithm at 10-14 weeks' gestation.

次要结局

  • Correlation between corpus luteal function and placental volume at 10-14 weeks(Visit 1 (<8 weeks) and Visit 2 (10-14 weeks))
  • Correlation between corpus luteum function and placental vascularity index at 10-14 weeks(Visit 1 (<8 weeks) and Visit 2 (10-14 weeks))
  • Incidence of pre-eclampsia(These outcomes will be collected via telephone calls and medical records at the following weeks of pregnancy: Weeks 18-21 (usual care [UC] visit 1 - routine hospital attendance for anomaly scan), delivery and up to 4-6 weeks post delivery)
  • Incidence of fetal growth restriction(These outcomes will be collected via telephone calls and medical records at the following weeks of pregnancy: Weeks 18-21 (usual care [UC] visit 1 - routine hospital attendance for anomaly scan), delivery and up to 4-6 weeks post delivery)
  • Incidence of preterm birth(At delivery (≥24 weeks))
  • Birth weight(At delivery)
  • Association between corpus luteal function and placental dysfunction(These outcomes will be collected via telephone calls and medical records at the following weeks of pregnancy: Weeks 18-21 (usual care [UC] visit 1 - routine hospital attendance for anomaly scan), delivery and up to 4-6 weeks post delivery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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