About this trial
National multicentric registry of a cohort of patient with suffering parietal endometriosis, carried out by a multidisciplinary radiosurgery team
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Presence of parietal endometriosis: with suggestive clinical and imaging criteria (MRI and ultrasound)
Symptomatic parietal endometriosis (VAS > 3 OR bothersome bleeding OR reported impact on quality of life)
Disqualifiers
Endometriosis not affecting the anterior wall of the abdomen (as deep pelvic muscle: ilio-psoas, obturators, perineal, ischio-anal fossa)
Minor patient (< 18 years)
Pregnant patient at any trimester
Patient with hemostasis disorders (constitutional or acquired)
Trial population
patient with endomecriosis at least 18 years of age who will be oer are treate by cryo ablation or surgical treatement
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
creation of a national registry for the removal of nodules by cryoablation or surgery for parietal endometriosis
number of Endometriosis 's patient treat by cryoablation or surgical
Secondary outcomes
Characterize the epidemiology of parietal endometriosis nodules
average of parietal endometriosis nodules
Characterize the epidemiology of parietal endometriosis nodules
average of parietal endometriosis nodules
To assess the impact of hormone treatment on parietal endometriosis
number of hormone treatment on parietal endometriosis
Assess the demographic distribution of parietal endometriosis
compare the size of of endometriosis nodules pre- and post-treatment
Sponsors and contacts
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