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Clinical Trials/NCT03899935
NCT03899935
Completed
Not Applicable

Feasibility and Safety of Endometriosis Laparoscopic Removal in Obese Patients: a Propensity Score Method Analysis

IRCCS Azienda Ospedaliero-Universitaria di Bologna1 site in 1 country1,230 target enrollmentJanuary 1, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Enrollment
1230
Locations
1
Primary Endpoint
Operative time
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Evaluation of surgical outcomes of endometriosis laparoscopic surgery in obese patients.

Detailed Description

Obesity may influence surgical variables such as operative time, laparotomic conversion rate and intraoperative and postoperative complication rate. Moreover, it might influence the hospital length of stay. For that reason, the study aims to compare a group of obese patients with a non-obese group of patients about these topics.

Registry
clinicaltrials.gov
Start Date
January 1, 2010
End Date
December 31, 2016
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Renato Seracchioli

Principal Investigator

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Eligibility Criteria

Inclusion Criteria

  • Obese patients undergoing endometriosis laparoscopic treatment
  • Obteined Informed Consensus

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Operative time

Time Frame: Intraoperative: from the skin incision to the skin suture

Comparison of operative time, expressed in minutes, between Group A and Group B

Secondary Outcomes

  • Laparotomic conversion rate(Intraoperative)
  • Hospital length of stay(Postoperative: from surgery to hospitalization discharge, assessed up to 30 days after surgery.)
  • Postoperative complication rate(Postoperative: from surgery to hospitalization discharge, assessed up to 30 days after surgery.)
  • Intraoperative complication rate(Intraoperative)

Study Sites (1)

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