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Laparoscopic Eradication of Deep Endometriosis With Nerve-sparing Rectosigmoid Segmental Resection (RSRES_NERVSP)

Laparoscopic Eradication of Deep Endometriosis With Nerve-sparing Rectosigmoid Segmental Resection: a Comparative Retrospective Analysis (RSRES_NERVSP)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05682690
Acronym
RSRES_NERVSP
Enrollment
3072
Registered
2023-01-12
Start date
2022-10-01
Completion date
2022-10-10
Last updated
2023-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Brief summary

This is a single-center, retrospective case-control study. All consecutive women who underwent classic and nerve-sparing segmental rectosigmoid resection between January 2005 and June 2022 will be included. In the majority of cases classic segmental rectosigmoid resection was done between January 2005 and December 2010. Nerve-sparing segmental rectosigmoid resection has been increasingly employed since January 2011 until now. Preoperative (anamnestic, physical objective, and ultrasonographic data), surgical and postoperative data of the patients included in this study will be analyzed. In particular, postoperative data will be obtained by analyzing reports of follow-up visits, which are routinely done at our institution at 1, 6, 12 months and then every year following the surgical procedures.

Interventions

None listed

Sponsors

IRCCS Sacro Cuore Don Calabria di Negrar
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum

Inclusion criteria

* consecutive women who underwent classic and nerve-sparing segmental rectosigmoid resection between January 2005 and June 2022 * age more than 18 years.

Exclusion criteria

* diagnosis of other/concomitant preoperative and/or postoperative medical or surgical conditions altering pelvic organ function (i.e. multiple sclerosis, irritable bowel syndrome); * age \<18 years.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients having long-term postoperative complications12 months after the surgical proceduresNumber of patients having short-term postoperative complications evaluated by clinical data stored in the hospital medical electronic register at the follow-up visits
Number of patients having intraoperative complicationsDuring the surgical proceduresNumber of patients having intraoperative complications evaluated by surgical data stored in the hospital medical electronic register
Number of patients having short-term postoperative complications3 months after the surgical proceduresNumber of patients having short-term postoperative complications evaluated by clinical data stored in the hospital medical electronic register at the follow-up visits
Number of patients having middle-term postoperative complications6 months after the surgical proceduresNumber of patients having short-term postoperative complications evaluated by clinical data stored in the hospital medical electronic register at the follow-up visits

Secondary

MeasureTime frameDescription
Intraoperative blood loss (ml)During the surgical proceduresIntraoperative blood loss (ml) evaluated by surgical data stored in the hospital medical electronic register
Number of patients having an intraoperative laparotomic conversionDuring the surgical proceduresIntraoperative blood loss (ml) evaluated by surgical data stored in the hospital medical electronic register
Operative time (min)During the surgical proceduresOperative time (min) evaluated by surgical data stored in the hospital medical electronic register
Number of patients undergoing a concomitant additional surgical procedureDuring the surgical proceduresNumber of patients undergoing a concomitant additional surgical procedure evaluated by surgical data stored in the hospital medical electronic register

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026