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

S

Scientific Institute for Research Hospitalization and Healthcare (IRCCS)

Status

Not yet enrolling

Conditions

Deep Endometriosis

Study type

Observational

Funder types

Other

Identifiers

NCT06826378
ARISTOTLE23

Details and patient eligibility

About

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

Full description

Surgery is the treatment of choice for deep endometriosis with bowel involvement and endometriosis nodules will be treated by segmental resection and subsequent anastomosis packing. Anastomosis packing with a totally intracorporeal approach may be a successful solution to reduce some of the complications after discoid or segmental resection with conventional laparotomic approach for extracorporeal anastomosis.

Setting up the colorectal anastomosis with a totally intracorporeal approach represents a surgical method that has been recently introduced but is already approved in terms of safety and reproducibility. However, experience with this technique is currently limited and there is no established consensus regarding patient suitability or data on longer-term outcomes. New studies are therefore needed to further validate the technique and to fully assess its long-term benefits resulting in increased quality of life for operated patients or to identify any associated complications.

The aim of the study is therefore to describe the impact on the quality of life (in terms of functional recovery and gastrointestinal symptoms) of segmental resection surgery in patients with intestinal endometriosis who underwent either a totally intracorporeal or extracorporeal procedure. In addition, the aim is to detect any differences in the duration of the operating time, compare the duration of the postoperative hospital stay and determine the success rate of the totally intracorporeal procedure

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 54 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

Diego Raimondo, MD; Stefano Ferla, MD

Data sourced from clinicaltrials.gov

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