Assessing the prevalence of endometriosis and adenomyosis in women seeking fertility preservation
Study of the Prevalence of Endometriosis and Adenomyosis in Women of Childbearing Age Consulting for Non-medical Oocyte Self-preservation
This study is trying to find out how common endometriosis and adenomyosis are in women who want to preserve their fertility and see how these conditions affect their mental health and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 29 Years to 37 Years |
| Sex | Female |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris, Île-de-France Region) |
| Trial ID | NCT06211569 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate how common adenomyosis and endometriosis are among women consulting for elective fertility preservation. Using transvaginal pelvic ultrasound, the study will diagnose these conditions and compare imaging results with clinical data, including patient characteristics and symptoms. Additionally, the study will assess the impact of these conditions on anxiety, depression, and quality of life. The goal is to improve understanding of the prevalence and correlation of these pathologies in reproductive-age women.
Who should consider this trial
Good fit: Ideal candidates are women aged 29 to 37 who are consulting for non-medical fertility preservation.
Not a fit: Patients who are pregnant or have known malformations of the genital tract may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of endometriosis and adenomyosis, leading to better treatment options and preventive strategies for women facing fertility issues.
How similar studies have performed: While the prevalence of these conditions has been studied, this specific approach using imaging and psychological assessments in the context of fertility preservation is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Woman aged between 29 and 37 * Consultant for non-medical fertility preservation in the Reproductive Medicine Unit Port Royal, Cochin * Informed and not opposed to this research * Affiliated to a social security scheme Exclusion Criteria: * Pregnant women * Refusing to take part in the study * Under court protection, curatorship or guardianship * Women with a known malformation of the genital tract
Where this trial is running
Paris, Île-de-France Region
- Gynécologie Obstétrique II et médecine de la reproduction, Hôpital Cochin, Port Royal — Paris, Île-de-France Region, France (Recruiting)
Study contacts
- Study coordinator: Mathilde BOURDON, MD
- Email: mathilde.bourdon@aphp.fr
- Phone: 00331 58 41 39 20
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.