HerResolve™ in Detecting the Presence of Endometriosis Among Symptomatic Women
Launched by CHINESE UNIVERSITY OF HONG KONG · May 28, 2025
Trial Information
Current as of July 23, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The HerResolve™ clinical trial is studying a new way to detect endometriosis, a common condition that affects many women and can cause severe pelvic pain and difficulties with fertility. This trial is aimed at women aged 18 to 49 who have symptoms like pelvic pain or unusual bleeding and are scheduled for a type of surgery called laparoscopy. During this surgery, doctors will look for signs of endometriosis and take samples to confirm its presence or absence.
To participate, women must be able to provide consent and have their medical history reviewed. They should not have certain health issues, such as cancer, or be pregnant. Participants will have blood drawn at specific times during their menstrual cycle, and the study aims to gather important information to help improve how endometriosis is diagnosed. It's important to note that the trial is not yet recruiting participants, but it hopes to shed light on this challenging condition and offer better solutions for those affected.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Females aged 18 to 49 with mild to severe symptoms of pelvic pain and/or abnormal bleeding.
- • Diagnostic laparoscopy is scheduled with histology on any visually suspected endometriosis, and all reports (surgical and pathology) to confirm a positive result. If no visually suspicious endometriotic lesions are seen, biopsies from random areas during the laparoscopy procedure to confirm a negative histopathology result.
- • Blood drawn during secretory or proliferative phase of the menstrual cycle
- • Provide written informed consent to participate in the study and provide medical history on medications.
- Exclusion Criteria:
- • Patients who object to medical history collection and data requests
- • Patients with cancer and/or undergoing chemotherapy and/or radiotherapy
- • Patients who are unable or do not undergo laparoscopic surgery
- • Patients participating in additional interventional clinical studies
- • Pregnant, lactating, or subjects who are not healthy enough for blood donation.
- • Blood drawn during menses or ovulation phase of menstrual cycle
- • Females who are post-menopausa
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, Shatin, Hong Kong
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported