NCT07472842

Brief Summary

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

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 25, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

October 16, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2026

Completed
2 months until next milestone

First Posted

Study publicly available on registry

March 16, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2026

Completed
Last Updated

March 16, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

August 25, 2025

Last Update Submit

March 12, 2026

Conditions

EndometriosisPelvic Pain SyndromeChronic Gynaecological Disease

Keywords

infertilitydysmenorrheapelvic pain

Outcome Measures

Primary Outcomes (4)

  • 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

Study Arms (1)

Impact of emergency room care on endometriosis or its diagnosis

OTHER
Diagnostic Test: Emergency care for endometriosis

Interventions

Emergency care for endometriosisDIAGNOSTIC_TEST

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

Impact of emergency room care on endometriosis or its diagnosis

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHI Créteil

Créteil, 94000, France

RECRUITING

MeSH Terms

Conditions

EndometriosisInfertilityDysmenorrheaPelvic Pain

Condition Hierarchy (Ancestors)

Genital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesMenstruation DisturbancesPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Central Study Contacts

Yann SALHI, MD

CONTACT

01 57 02 20 00yann.salhi@chicreteil.fr

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 25, 2025

First Posted

March 16, 2026

Study Start

October 16, 2025

Primary Completion

January 15, 2026

Study Completion

July 15, 2026

Last Updated

March 16, 2026

Record last verified: 2026-03

Locations

FR(1)