Clinical Trials in Italy / NCT06826378
Starting soon
Observational
Patients Undergoing Total Intracorporeal or Extracorporeal Anastomosis After Segmental Resection for Deep Endometriosis
NCT06826378 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Deep Endometriosis
Study summary
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
Inclusion Criteria:
* 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
Exclusion Criteria:
* Patients with a known concomitant inflammatory bowel syndrome (inflammatory bowel syndrome)
* Patients undergoing emergency/emergency surgery
Primary outcome measure(s)
- 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 — During the preoperative evaluation and at 3 months after surgery as part of the postoperative follow-up visit
Evaluation by scoring the validated Low Anterior Resection Syndrome score questionnaire
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06826378 on ClinicalTrials.gov ↗ ← All trials in Italy