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Recruiting NCT07472842

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

No phase Interventional Endometriosis Pelvic Pain Syndrome Chronic Gynaecological Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Emergency care for endometriosis.
Who it may be relevant to
Registry conditions: Endometriosis, Pelvic Pain Syndrome, Chronic Gynaecological Disease. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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. 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.

Interventions

  • 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

Primary outcome measures

  • Assessing the impact of treatment in gynecological emergency departments on patients with endometriosis or suspected endometriosis [Time frame: At 3 months]
  • Assessing the impact of treatment in gynecological emergency departments on patients with endometriosis or suspected endometriosis [Time frame: At 3 months]
  • Assessing the impact of treatment in gynecological emergency departments on patients endometriosis or suspected endometriosis [Time frame: At 3 months]
  • Assessing the impact of deprivation on the future of patients after consultation at gynaecological emergency departments. [Time frame: At 3 months]

Eligibility 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

France · 1 center
  • CHI Créteil — Créteil

Identifiers

NCT: NCT07472842 · ENDO URG

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗