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Search / Trial NCT03925311

Transcriptome Profiling and Endometrial Receptivity

Launched by CHINESE UNIVERSITY OF HONG KONG · Apr 18, 2019

Trial Information

Current as of August 22, 2025

Recruiting

Keywords

Transcriptome Endometrial Receptivity

ClinConnect Summary

This clinical trial is focused on understanding how certain biochemical markers in the body relate to the best time for a woman to become pregnant, known as the "window of implantation" (WOI). Researchers will collect blood samples and perform a small procedure called an endometrial biopsy, where a tiny sample of the lining of the uterus is taken, at specific times during a woman’s cycle to gather important information.

To participate, women aged 20 to 40 years old may be eligible, but those with certain uterine issues, such as fibroids, or other specific conditions will not be able to join. If you choose to participate, you can expect to provide blood samples and undergo the biopsy at scheduled visits. This study is currently looking for participants, so if you meet the age criteria and are interested in contributing to this important research, you may want to learn more about it!

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Age 20-40 years.
  • Exclusion Criteria:
  • Uncorrected uterine anomalies, such as septate or bicornuate uterus, fibroids (submucous/intramural).
  • Intrauterine adhesions.
  • Adenomyosis.

About Chinese University Of Hong Kong

The Chinese University of Hong Kong (CUHK) is a prestigious research institution renowned for its commitment to advancing medical science and improving healthcare outcomes. As a clinical trial sponsor, CUHK leverages its extensive academic resources and interdisciplinary expertise to conduct innovative research that addresses critical health challenges. The university fosters collaboration among leading researchers, healthcare professionals, and industry partners, ensuring rigorous study design and implementation. CUHK is dedicated to upholding the highest ethical standards in clinical research, with a focus on translating findings into tangible benefits for patients and the broader community.

Locations

Hong Kong, , Hong Kong

Patients applied

0 patients applied

Trial Officials

Pui Wah Jacqueline Chung, MBBS

Principal Investigator

Chinese University of Hong Kong

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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