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Search / Trial NCT06311812

Retrospective Review on Uterovaginal Anomalies

Launched by CHINESE UNIVERSITY OF HONG KONG · Mar 13, 2024

Trial Information

Current as of November 08, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at the surgical outcomes of women who have had surgery for conditions related to uterovaginal anomalies, which are abnormalities affecting the uterus and vagina. Researchers will review the medical records of these patients from the Prince of Wales Hospital, focusing on the results of their surgeries to gather important data for analysis.

To be eligible for this study, participants must be female and have been diagnosed with a uterovaginal anomaly while receiving care at the hospital since the year 2000. There are no specific exclusions, meaning anyone meeting the inclusion criteria can participate. If you or someone you know qualifies, you can expect that your past medical records will be examined to help improve understanding of these conditions and the effectiveness of surgical treatments. This study is currently recruiting participants, so it's a great opportunity to contribute to valuable research in this area.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • All patients who attended the Prince of Wales Hospital with the diagnosis of uterovaginal anomaly since 2000
  • Exclusion Criteria:
  • Nil

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

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported