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Clinical Trial NCT07472842 for Endometriosis, Pelvic Pain Syndrome, Chronic Gynaecological Disease is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Study on the Outcomes of Patients Treated in Gynecological Emergency Departments for Pelvic Endometriosis or Suspected Pelvic Endometriosis 200

Recruiting
Clinical Trial NCT07472842 is an interventional study for Endometriosis, Pelvic Pain Syndrome, Chronic Gynaecological Disease that is recruiting. It started on 16 October 2025 with plans to enroll 200 participants. Led by Centre Hospitalier Intercommunal Creteil, it is expected to complete by 15 July 2026. The latest data from ClinicalTrials.gov was last updated on 16 March 2026.
Brief Summary
Adult patients consulting the gynecological emergency department of CHI Créteil during the inclusion period for endometriosis or symptoms suggestive of 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. S...Show More
Official Title

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

Conditions
EndometriosisPelvic Pain SyndromeChronic Gynaecological Disease
Other Study IDs
  • ENDO URG
NCT ID Number
NCT07472842
Start Date (Actual)
2025-10-16
Last Update Posted
2026-03-16
Completion Date (Estimated)
2026-07-15
Enrollment (Estimated)
200
Study Type
Interventional
PHASE
N/A
Status
Recruiting
Keywords
infertility
dysmenorrhea
pelvic pain
Primary Purpose
Diagnostic
Design Allocation
N/A
Interventional Model
Single Group
Masking
None (Open Label)
Arms / Interventions
Participant Group/ArmIntervention/Treatment
OtherImpact of emergency room care on endometriosis or its diagnosis
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
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime 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
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
Female
  • 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

  • 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
Centre Hospitalier Intercommunal Creteil logoCentre Hospitalier Intercommunal Creteil
Study Central Contact
Contact: Yann SALHI, MD, 01 57 02 20 00, [email protected]
1 Study Locations in 1 Countries
CHI Créteil, Créteil, 94000, France
Yann SAHLI, MD, Contact, 01 57 02 20 00, [email protected]
Recruiting