Actively Recruiting

Phase Not Applicable
Age: 18Years - 49Years
FEMALE
Healthy Volunteers
NCT07006987

HerResolve™ in Detecting the Presence of Endometriosis Among Symptomatic Women

Led by Chinese University of Hong Kong · Updated on 2025-12-03

100

Participants Needed

1

Research Sites

606 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Endometriosis (EMS) is a common gynecological disease that affects 176 million girls and women globally. EMS affects 5-10% of women and adolescents within the reproductive age range of 15-49 years, and for those facing infertility, this figure may climb up to 50%. EMS can start at the first menstrual period and last until menopause. Shockingly, between 50% and 80% of women grappling with pelvic pain are found to have EMS. The formation of scar tissue (adhesions, fibrosis) within the pelvis and other parts of the body can cause severe pain and lead to infertility.

CONDITIONS

Official Title

HerResolve™ in Detecting the Presence of Endometriosis Among Symptomatic Women

Who Can Participate

Age: 18Years - 49Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Females aged 18 to 49 with mild to severe symptoms of pelvic pain and/or abnormal bleeding.
  • Scheduled for diagnostic laparoscopy with histology to confirm presence or absence of endometriosis.
  • Blood drawn during secretory or proliferative phase of menstrual cycle.
  • Provide written informed consent and medical history on medications.
Not Eligible

You will not qualify if you...

  • Patients who refuse medical history collection or data requests.
  • Patients with cancer or undergoing chemotherapy or radiotherapy.
  • Patients unable or unwilling to undergo laparoscopic surgery.
  • Patients participating in other interventional clinical studies.
  • Pregnant, lactating, or not healthy enough for blood donation.
  • Blood drawn during menses or ovulation phase of menstrual cycle.
  • Females who are post-menopausal.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Obstetrics & Gynaecology The Chinese University of Hong Kong

Hong Kong, China

Actively Recruiting

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Research Team

E

Elaine Ng

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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