ConditionDeep Endometriosis
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-54
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
About this trial
Impact on the quality of life (in terms of functional recovery and gastrointestinal symptoms) of segmental resection surgery in patients with intestinal endometriosis undergoing either a totally intracorporeal or extracorporeal procedure
Eligibility criteria
Qualifiers
Women between 18 and 54 years of age
Diagnosis, by instrumental examination such as transvaginal ultrasound, of deep endometriosis with suspected intestinal involvement
Intraoperative indication for segmental resection for intestinal endometriosis
Obtaining informed consent for study participation and data processing
Disqualifiers
Patients with a known concomitant inflammatory bowel syndrome (inflammatory bowel syndrome)
Patients undergoing emergency/emergency surgery
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov