Outcomes after emergency gynecology care for pelvic endometriosis or suspected endometriosis
Official title: Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis
Run by Centre Hospitalier Intercommunal Creteil · NCT07472842 · Data updated 2026-11-12
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
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 200 (estimated) |
| Sponsor | Centre Hospitalier Intercommunal Creteil Academic / other |
| Locations | 1 site (Créteil) |
| Status | Recruiting |
| Started | October 16, 2025 |
| Main results expected | January 15, 2026 |
| Study ends | November 15, 2026 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT07472842 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a 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.
✕Probably 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.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: 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.
Who can join: the full rules
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 it's running
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CHI Créteil
Créteil, France Recruiting
Study contacts
- Study coordinator: Yann SALHI, MD
- Email: yann.salhi@chicreteil.fr
- Phone: 01 57 02 20 00
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Good pain consultation for endometriosis
This trial will test whether adding a 'good pain consultation' with early biopsychosocial pain education to usual care helps biological women with endometriosis manage pain and improve quality of life.
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Comparing different techniques to treat endometriosis
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A fiber-based supplement is being tested to see if it is safe and helps with gut and vaginal microbiomes and digestive symptoms in women with endometriosis.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.