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OpenTrials
Completed

NCT Number: NCT03401918

Assessing the Endometrial Environment in Recurrent Pregnancy Loss and Unexplained Infertility

The purpose of this study is to determine if patients with recurrent pregnancy loss or unexplained infertility have an altered uterine gene expression or uterine microbiome (micro-organism composition) during the window of embryo implantation. Furthermore we would like to assess for women with an abnormal uterine gene expression whether vaginal progesterone medication improves or alters gene expression and for women with an abnormal microbiome whether antibiotic treatment followed by probiotic treatment normalizes the microbiome.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Reproductive Endocrinology and Infertility Center at Stanford University

Sunnyvale, California, 94087, United States

About this study

Recurrent pregnancy loss and unexplained infertility are emotional and difficult diagnoses. Despite a thorough medical investigation, many cases of recurrent pregnancy loss and infertility remain unexplained. Understanding endometrial factors that may contribute to these diseases may lead to improved treatment options in the future. The purpose of this study is to determine if patients with recurrent pregnancy loss or unexplained infertility have an altered uterine gene expression or uterine microbiome (micro-organism composition) during the window of embryo implantation. Furthermore we would like to assess for women with an abnormal uterine gene expression whether vaginal progesterone medication improves or alters gene expression and for women with an abnormal microbiome whether antibiotic treatment followed by probiotic treatment normalizes the microbiome.

A standard evaluation for infertility includes a uterine cavity evaluation, evaluation for ovarian reserve testing, and for patients with recurrent pregnancy loss parental testing for uterine infection, chromosome analysis, autoimmune and thyroid screening. This standard workup, however, does not include a molecular or microbial assessment of the endometrium. Endometrial factors may contribute to unexplained infertility or recurrent pregnancy loss however the extent of this is unknown.

We are recruiting patients who have recurrent pregnancy loss, unexplained infertility, and healthy control patients who have had a term delivery in order to compare differences between these groups.

Subjects will undergo an endometrial biopsy that will specifically test the receptivity of your endometrium as well as identify the bacterial composition of the uterine environment (microbiome). The endometrial receptivity array and microbiome testing will be performed at no cost. The endometrial receptivity array provides information on the receptivity of a patient's endometrium to the implantation of an embryo. This may yield additional information regarding the etiology of a patient's infertility and/or recurrent pregnancy loss. If this testing is abnormal we may repeat the biopsy after vaginal progesterone supplementation to see if this normalizes the results. If the microbiome is abnormal we may repeat the biopsy after oral antibiotics and vaginal probiotics to see if this normalizes your microbiome results.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion/Exclusion Criteria:

  • Recurrent Pregnancy Loss

Inclusion:

  • Age 18-45
  • 3 or more SABs including biochemical pregnancies OR 2 or more SABs if one is documented to be euploid

Exclusion:

  • irregular menstrual cycles
  • Submucosal fibroid >3cm
  • Stage 3-4 endometriosis
  • BMI >40
  • IUD within the last 3 months
  • Unexplained infertility Patients

Inclusion:

  • TTC x >= 1 year
  • At least one SA with TMS >10 mil within last 2 years
  • At least one patent fallopian tube documented by HSG or SHG
  • Cycle length 25-35 days

Exclusion:

  • Irregular menstrual cycles
  • Submucosal fibroid >3cm
  • Stage 3-4 endometriosis
  • BMI >40
  • IUD within the last 3 months
  • Less then 2 SABs including biochemical pregnancies
  • Healthy control patients

Inclusion:

  • Patients who present for fertility preservation, sex selection, same sex couples needing fertility care, preconception counseling
  • 1 or more live births

Exclusion:

  • Irregular menstrual cycles
  • Submucosal fibroid >3cm
  • Stage 3-4 endometriosis
  • BMI >40
  • IUD within the last 3 months
  • Less then 2 SABs including biochemical pregnancies
  • No history of RPL or infertility

Treatment and study plan

Uterine ERA and microbiome testing

Diagnostic Test

Uterine fluid and endometrial biopsy collection to test uterine endometrial receptivity array and microbiome.

Oral antibiotics and vaginal probiotics

Drug

For subjects with abnormal microbiome results, oral antibiotics and vaginal probiotic treatment will be offered followed by a repeat uterine microbiome biopsy.

Primary outcomes

  1. Abnormal Microbiome Bacterial Sequencing

    Time frame: 1 month

    The primary outcome will abnormal microbiome results. An abnormal microbiome will be defined as less then 90% lactobacilli on DNA sequencing

  2. Abnormal Endometrial Receptivity Array

    Time frame: 1 month

    The second primary outcome will be abnormal endometrial receptivity array defined as non-receptive (pre or post receptive) based on RNA sequencing of an endometrial gene array.

  3. Normalized Microbiome Bacterial Sequencing

    Time frame: 3-6 months

    The primary outcome will be normal microbiome results defined as >90% lactobacilli after oral antibiotics and vaginal probiotics after initially abnormal microbiome results

  4. Normalized Endometrial Receptivity Array

    Time frame: 3-6 months

    The primary outcome will be normal endometrial receptivity array results defined as receptive after luteal phase progesterone support after initially abnormal endometrial receptivity array results

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • Instituto Valenciano de Infertilidad, IVI VALENCIA

Registry information

Important dates

Study start
2017
Primary completion
2021
Study completion
2021
First posted
Jan 17, 2018
Registry last updated
Apr 1, 2025

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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