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Completed

NCT Number: NCT04107129

Predicting Endometrial Receptivity for Optimal Reproductive Management

The purpose of this study is to understand why some women are infertile (unable to conceive a child). The investigators hope to learn if an endometrial biopsy after egg retrieval is feasible for detecting biomarkers for endometriosis and predicting implantation and pregnancy rate after embryo transfer.

This study design will provide for the first time, an opportunity to compare endometrial biopsy material from hyperstimulated (gonadotropin treated) subjects after egg retrieval. If successful, it would provide a new protocol for women with unexplained infertility or those with known endometriosis to avoid poor IVF outcomes.

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Key information

Age range

18 year–42 year

Sex eligibility

Female

Study type

Observational

Primary location

Stanford Fertility and Reproductive Health

Sunnyvale, California, 94087, United States

About this study

The investigators will recruit 100 women who are undergoing IVF with egg retrieval and delayed embryo transfer to consent to endometrial biopsy 1 week after egg retrieval. Currently most women in the Stanford's IVF program undergo egg retrieval with delayed embryo transfer (ET) with preimplantation genetic testing of embryos. This delay allows most to avoid the condition known as ovarian hyperstimulation and allows time for genetic screening (PGT-A) performed on embryos. Such a delay also opens the window for endometrial assessment for proteins like SIRT1 and BCL6 that have been suggested to be associated with endometriosis. Endometriosis is thought to cause IVF failure (Littman et al., 2002); by treating endometriosis in the future, clinicians might avoid IVF failure due to an unexpected non-receptive endometrium (Littman et al., 2002). This study design will provide for the first time, an opportunity to compare endometrial biopsy material from hyperstimulated (gonadotropin treated) subjects after egg retrieval. If successful, it would provide a new protocol for women with unexplained infertility or those with known endometriosis to avoid poor IVF outcomes.

There is some evidence that endometrial scratching (biopsy) may enhance embryo attachment in future cycles (Vitagliano et al., 2018), although not all studies agree (Lensen et al., 2019). The endometrial biopsy taken in the secretory phase will be tested for BCL6 and SIRT1 expression, two proteins highly associated with the presence of endometriosis (Yoo et al., 2017). The samples of endometrium will be processed (put into formalin and paraffin blocks or saved in RNA later and not be analyzed until after completion of the ART cycle. Patients as well as the clinicians will be blinded to results and until the conclusion of the ART cycle following embryo transfer and subsequent pregnancy testing. This will be done to avoid interfering with the current ART cycle and to avoid the introduction of bias. Patients will be provided with test results after completion of the first embryo transfer if they wish to know.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age - 18 to 42
  • AMH ≥ 1
  • Planning to undergo IVF with delayed embryo transfer
  • Must have blastocyst(s) by day 6 that were biopsied for PGT-A
  • BMI 18-35

Exclusion criteria

  • Uterine fibroids > 4 cm in size
  • Polycystic ovary syndrome (PCOS) according with the Rotterdam criteria.
  • Ovarian failure and subjects receiving donor oocytes/embryos
  • Anti-cardiolipid and/or lupus anti-coagulant abnormalities by history
  • Diabetes mellitus (Type I or Type II)
  • Untreated hypothyroidism
  • Hyperprolactinemia
  • Uncorrected uterine anomaly

Treatment and study plan

endometrial biopsy

Procedure

An endometrial biopsy is the removal of a small piece of tissue from the endometrium, which is the lining of the uterus. Endometrial tissue will be tested for BCL6 and SIRT1 Biomarkers

Euploid embryo transfer

Other

Patients undergoing IVF and Preimplantation genetic testing will undergo delayed euploid frozen embryo transfer per clinical protocol and standard of care.

Blood sample

Diagnostic Test

Estradiol and Progesterone levels in the blood will be checked

Primary outcomes

  1. SIRT1 gene expression in the endometrium

    Time frame: 2-3 years

    Endometrial biopsy specimens will be stained for SIRT1 using immunostaining and Hscore assignment.

Secondary outcomes

  1. BCL6 expression in the endometrium

    Time frame: 2-3 years

    Endometrial biopsy specimens will be stained for BCL6 using immunostaining and Hscore assignment.

  2. Number of patients who have a positive pregnancy test (HCG level > 5) 9 days after embryo transfer

    Time frame: 2-3 years

    pregnancy rate

  3. Number of embryo transfers that lead to live births

    Time frame: 2-3 years

    live birth rate

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Registry information

Official study title

Predicting Endometrial Receptivity for Optimal Reproductive Management (PERFORM)

Acronym: PERFORM

Important dates

Study start
2020
Primary completion
2023
Study completion
2024
First posted
Sep 27, 2019
Registry last updated
Aug 14, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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