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
Locations
1Sponsors and collaborators
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead sponsor