Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis

Adult patients consulting the gynecological emergency department of CHI Créteil during the inclusion period for endometriosis or symptoms suggestive of endometriosis

Study Overview

• Status: Recruiting
• Conditions: Endometriosis; Pelvic Pain Syndrome; Chronic Gynaecological Disease
• Intervention / Treatment: Diagnostic test: Emergency care for endometriosis

Detailed Description

Endometriosis is defined as the presence outside the uterine cavity of tissue similar to the uterine mucosa, which will be affected by hormonal changes during each subsequent menstrual cycle. Endometriosis is thus responsible for pelvic pain, which can be particularly incapacitating, as well as other symptoms depending on the location of the lesions. In some cases, endometriosis is also responsible for infertility. Symptoms have a considerable impact on the quality of life of sufferers, affecting not only their personal and marital lives, but also their professional and social lives.

• Study Type: Interventional
• Enrollment (Estimated): 200
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Yann SALHI, MD; Phone Number: 8456 01 57 02 20 00; Email: yann.salhi@chicreteil.fr

Study Locations

• France
  • Créteil, France, 94000
    • Recruiting
    • Chi Creteil
    • Contact: Yann SAHLI, MD; Phone Number: 01 57 02 20 00; Email: yann.sahli@chicreteil.fr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Diagnostic
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Impact of emergency room care on endometriosis or its diagnosis	Diagnostic test: Emergency care for endometriosis; Emergency care for endometriosis; Introduction of specific treatment for endometriosis; Scheduled or completed specialist consultation (gynecologist, surgeon, midwife, radiologist); Pelvic imaging examination scheduled or completed since the gynecological emergency consultation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessing the impact of treatment in gynecological emergency departments on patients with endometriosis or suspected endometriosis	Composite criteria : number of specific hormonal or analgesic treatment introduiced for endometriosis according to ESHRE guideline endometriosis	At 3 months
Assessing the impact of treatment in gynecological emergency departments on patients with endometriosis or suspected endometriosis	Composite criteria : number of scheduled or completed specialist consultation (gynaecologist, surgeon, midwife, radiologist)	At 3 months
Assessing the impact of treatment in gynecological emergency departments on patients endometriosis or suspected endometriosis	Composite criteria : number of Pelvic imaging recommanded for diagnostic or follow up of endometriosis, according to ESHRE guideline, scheduled or completed since the gynecological emergency consultation	At 3 months
Assessing the impact of deprivation on the future of patients after consultation at gynaecological emergency departments.	EPICE Scores (Evaluation of Deprivation and Inequalities in Health Examination Centers)	At 3 months

Collaborators and Investigators

• Sponsor: Centre Hospitalier Intercommunal Creteil

Study record dates

Study Major Dates

• Study Start (Actual): October 16, 2025
• Primary Completion (Actual): January 15, 2026
• Study Completion (Estimated): July 15, 2026

Study Registration Dates

• First Submitted: August 25, 2025
• First Submitted That Met QC Criteria: March 12, 2026
• First Posted (Actual): March 16, 2026

Study Record Updates

• Last Update Posted (Actual): March 16, 2026
• Last Update Submitted That Met QC Criteria: March 12, 2026
• Last Verified: March 1, 2026

More Information

Terms related to this study

• Keywords: infertility; dysmenorrhea; pelvic pain
• Additional Relevant MeSH Terms: Urogenital Diseases; Genital Diseases; Pain; Neurologic Manifestations; Pathologic Processes; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Genital Diseases, Female; Menstruation Disturbances; Pathological Conditions, Signs and Symptoms; Signs and Symptoms; Infertility; Endometriosis; Pelvic Pain; Dysmenorrhea
• Other Study ID Numbers: ENDO URG

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No