Patients Undergoing Total Intracorporeal or Extracorporeal Anastomosis After Segmental Resection for Deep 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