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NCT Number: NCT04721899

Vitamin D and Endometrial Receptivity in Infertile Women

This is a prospective study comparing vaginal and endometrial biomarkers and the trophoblast spheroid attachment rate in women with fertility problems before and after taking Vitamin D for 8 weeks.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Observational

Primary location

Queen Mary Hospital

Hong Kong, 000000

Location status: Recruiting

Location contact

Jennifer KY Ko, MBBS, MRCOG

CONTACT

[email protected]

22554647

About this study

The aim of this study is to assess the effect of vitamin D supplementation on vaginal / endometrial biomarkers and endometrial receptivity in women with fertility problems.

Women will have vaginal swab and endometrial biopsy twice. The first endometrial biopsy is performed using a Pipelle sampler 7 days after luteinizing hormone surge (LH+7) at baseline and the attachment rate of the trophoblast spheroid onto the isolated endometrial epithelial cells will be assessed to assess endometrial receptivity at baseline. Implantation biomarkers will be checked.

They will take Vitamin D 50,000 IU once per week for 4 weeks, followed by 50,000 IU once every 2 weeks for 4 weeks. After 8 weeks of Vitamin D, a second vaginal swab and endometrial biopsy using a Pipelle sampler by standard technique will be collected from the patients 7 days after luteinizing hormone surge (LH+7) and the endometrial receptivity will be compared.

The laboratory staff will not know whether the patient is taking any vitamin D when performing the trophoblast spheroid attachment assay/ biomarkers.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age of women < 40years old
  • Normal uterine cavity as demonstrated by pelvic scanning with or without saline infusion sonogram or hysteroscopy
  • Regular ovulatory cycles

They will be divided into three groups:

  • RIF patients (n=35)- those who have failed to get pregnant after replacing four or more cleavage stage embryos or two or more blastocysts in two consecutive transfers.
  • RPL patients (n=35)- those who have failed in three pregnancies before 24 weeks of gestation and includes embryonic and fetal losses.
  • 'Infertile group'(n=35)- infertility except RIF and RPL, e.g. those seeking for preimplantation genetic testing, male factor infertility, unexplained infertility.

Exclusion criteria

  • History of any medical condition or medications that may predispose to vitamin D sensitivity, altered vitamin D metabolism and/ or hypercalcemia, including active tuberculosis or current therapy for tuberculosis, sarcoidosis, history of renal/ ureteral stones, parathyroid disease, renal or liver failure or current use of anti-convulsants
  • Taking vitamin D supplement
  • Endometrial polyp or fibroid distorting the uterine cavity
  • Presence of hydrosalpinx not corrected surgically
  • Refusal to join the study
  • Discontinuation criteria-
  • If the woman becomes pregnant during the study
  • Pelvic inflammatory disease/ uterine perforation after endometrial biopsy
  • Vitamin D toxicity (hypercalcemia)
  • Withdrawal by patient

Treatment and study plan

Vitamin D

Dietary Supplement

Vitamin D 50,000 IU once per week for 4 weeks, followed by 50,000 IU once every 2 weeks for 4 weeks

Primary outcomes

  1. Change in endometrial receptivity

    Time frame: 8 weeks

    Assessed by the attachment rate of trophoblast spheroid attachment assay onto the isolated endometrial epithelial cells

Study contacts

Contact information is provided by the study sponsor or research team.

Jennifer KY Ko

CONTACT

[email protected]

22554647

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Official study title

Effect of Vitamin D on Vaginal / Endometrial Biomarkers and Endometrial Receptivity in Women With Fertility Problems

Important dates

Study start
2021
Primary completion
2025
Study completion
2026
First posted
Jan 25, 2021
Registry last updated
May 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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