Outcomes after emergency gynecology care for pelvic endometriosis or suspected endometriosis
Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis
This project will follow adults who come to a gynecological emergency department with known or suspected endometriosis to see what their outcomes are after emergency care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Centre Hospitalier Intercommunal Creteil Academic / other |
| Locations | 1 site (Créteil) |
| Trial ID | NCT07472842 on ClinicalTrials.gov |
What this trial studies
Adults presenting to the gynecological emergency department at CHI Créteil with known endometriosis or symptoms suggestive of endometriosis are enrolled during the inclusion period and receive standard emergency care. Clinical details at presentation and treatments provided are recorded, and patients complete a follow-up questionnaire at three months to capture pain, functional impact, and healthcare use. The protocol excludes minors, menopausal women, pregnant or breastfeeding patients, and those who cannot be contacted for follow-up. The study aims to characterize short-term outcomes and care pathways after emergency visits for endometriosis-related problems.
Who should consider this trial
Good fit: Ideal candidates are adults (18+) who speak French and present to the CHI Créteil gynecological emergency department with known endometriosis or symptoms suggestive of endometriosis.
Not a fit: Patients who are minors, menopausal, pregnant or breastfeeding, visiting for an unrelated reason, lacking social security affiliation, or unable to be contacted for the three-month questionnaire are unlikely to participate or benefit from this study.
Why it matters
Potential benefit: If successful, the results could help clinicians improve emergency management and follow-up plans for people with endometriosis, potentially reducing pain and disruptions to daily life.
How similar studies have performed: While many studies have described endometriosis symptoms and long-term management, relatively few have specifically tracked outcomes after gynecological emergency visits, so this emergency-focused approach is somewhat novel though it builds on established endometriosis research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria : * Adult patient (aged 18 or over) * Patient consulting the gynecological emergency department at Créteil Hospital for * Known endometriosis or * Symptoms suggestive of endometriosis: dysmenorrhea, pelvic pain, cyclic dysuria, dyspareunia, cyclic dyschezia, infertility, rectal bleeding, chest pain, catamenial hematuria * Patient who speaks French and is able to understand the information sheet Exclusion Criteria: * Minor or menopausal patient * Pregnant and breastfeeding patient * Other reason for consultation * Patient refusal * Patient not affiliated with a social security system * Patient cannot be contacted for the 3-months questionnaire
Where this trial is running
Créteil
- CHI Créteil — Créteil, France (Recruiting)
Study contacts
- Study coordinator: Yann SALHI, MD
- Email: yann.salhi@chicreteil.fr
- Phone: 01 57 02 20 00
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.