Actively Recruiting
Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis
Led by Centre Hospitalier Intercommunal Creteil · Updated on 2026-03-16
200
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on adult women visiting the gynecological emergency department for pelvic endometriosis or signs that suggest endometriosis. Endometriosis is a condition where tissue similar to the lining inside the uterus grows outside it, causing significant pelvic pain and other symptoms that can disrupt personal, social, and professional life. It can also lead to infertility, making the study important for understanding patient outcomes after emergency care. The study evaluates emergency care provided for endometriosis, including specific treatments introduced during the emergency visit, as well as planned or completed consultations with specialists such as gynecologists, surgeons, midwives, or radiologists. Participants may also undergo pelvic imaging exams scheduled or completed after the emergency consultation. This is an interventional study without masking, focusing on the impact of care received in the emergency department. Participants will be assessed on how emergency treatment affects their condition over a 3-month period. Researchers will collect data on symptoms and treatment impact, including the influence of social deprivation on patient outcomes. Women must complete questionnaires and follow-up evaluations at 3 months after their emergency visit. The study begins in October 2025 and continues until July 2026, with ongoing monitoring of patient experiences and outcomes.
CONDITIONS
Brief Title
Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient (aged 18 or over)
- Female patient consulting the gynecological emergency department at Cr�e9teil Hospital
- Known endometriosis or symptoms suggestive of endometriosis such as 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
You will not qualify if you...
- Minor or menopausal patient
- Pregnant and breastfeeding patient
- Consultation for reasons other than endometriosis
- Patient refusal to participate
- Patient not affiliated with a social security system
- Patient cannot be contacted for the 3-months questionnaire
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Day of emergency consultation
Participants receive emergency care and diagnostic assessments for endometriosis in the gynecological emergency department.
1 visit (in-person)
Duration - 3 months
Participants are followed for 3 months after emergency care to assess the impact of treatment and symptoms.
Follow-up assessments at 3 months
Trial Site Locations
Total: 1 location
1
CHI Créteil
Créteil, France, 94000
Actively Recruiting
Research Team
Y
Yann SALHI, MD
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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