Observational study on women with endometriosis and adenomyosis
Prospective Long Term Observational Study of Health Profile, Clinical Characteristics and Outcome of Patients Suffering From Endometriosis and Adenomyosis
This study is gathering health information from women with endometriosis and adenomyosis to see how their quality of life and reproductive health are affected, in hopes of finding better treatment options for different patient needs.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 880 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT04862000 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather health profiles of women suffering from endometriosis and adenomyosis through structured questionnaires that assess quality of life and reproductive health. The study will also collect sonographic characteristics and identify risk factors associated with severe disease. By analyzing this data, the investigators hope to propose optimal treatment modalities tailored to different patient groups, including those with and without fertility wishes. The study is conducted at a tertiary gynecology referral center with a high volume of patients affected by these conditions.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and older with histologically confirmed or sonographic evidence of endometriosis or adenomyosis.
Not a fit: Patients who are menopausal, refuse to participate, or are illiterate or mentally incapable may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and better quality of life for women suffering from endometriosis and adenomyosis.
How similar studies have performed: While there have been studies on endometriosis and adenomyosis, this specific observational approach focusing on health profiles and treatment modalities is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * with endometriosis or adenomyosis confirmed by ultrasound or MRI Exclusion Criteria: * refuse to participate in the study, less than 18 years old, menopausal, illiterate or mentally incapable
Where this trial is running
Hong Kong
- The Chinese University of Hong Kong — Hong Kong, Hong Kong (Recruiting)
Study contacts
- Principal investigator: Wen Ying Linda FUNG — Chinese University of Hong Kong
- Study coordinator: Wen Ying Linda FUNG
- Email: lindafung@cuhk.edu.hk
- Phone: (852) 55699192
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.