Patient's Experience and Choice Between Investigations for Endometrial Cancer in Postmenopausal Bleeding
Launched by CHINESE UNIVERSITY OF HONG KONG · Oct 30, 2017
Trial Information
Current as of April 25, 2025
Completed
Keywords
ClinConnect Summary
Endometrial cancer is the most common malignancy of the female genital tract in Hong Kong. It is estimated that around 10% of women experience postmenopausal bleeding. Around 90% of women with endometrial cancer initially presented with postmenopausal bleeding (PMB). The aim in the evaluation of PMB is to exclude underlying malignancy. Clinical tests to evaluate the endometrium include transvaginal ultrasound scanning (TVS) to measure endometrial thickness (ET), endometrial biopsy or sampling (ES), saline infusion sonography, and hysteroscopy. TVS ET or ES has been recommended as the first-...
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • postmenopausal woman
- • referrals for the symptom of PMB
- Exclusion Criteria:
- • dementia
- • mental retardation
Trial Officials
Wen Ying Fung
Principal Investigator
Chinese University of Hong Kong
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Hong Kong, , Hong Kong
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials