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NCT07919067Completed

Closure Versus Non-Closure of Working Ports in Laparoscopic Sleeve Gastrectomy

A Comparative Study Between Closure Versus Non-Closure of Working Ports in Laparoscopic Sleeve Gastrectomy: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 5 Nov 2026

Brief summary (registry, in English)

This randomized controlled trial compared closure versus non-closure of the fascia at the working port (trocar) sites during laparoscopic sleeve gastrectomy for severe obesity. A total of 160 adult patients undergoing laparoscopic sleeve gastrectomy at Kasr Al Ainy Hospital, Cairo University, were randomly allocated (1:1) to non-closure of the working ports (skin closure only) or fascial closure of the working ports using a fascial closure device. Patients were followed for one year for the development of port-site hernia. Postoperative pain was assessed with the Visual Analogue Scale (VAS) at one week and one month, and functional recovery with the Quality of Recovery-15 (QoR-15) score at one week.

Status (registry)
Completed
Study type
Interventional
Enrollment
160 (actual)
First submitted
31 Oct 2026
Start date
1 Oct 2024
Primary completion date
31 May 2026
Lead sponsor
Kasr El Aini Hospital
Diseases
Obesity
NCT number
NCT07919067

What you commit to

  • Study type: Interventional
  • Participants enrolled: 160
  • From 1 Oct 2024 to the primary completion date, 31 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Significant long-standing cardiac or pulmonary disease
  • Severe systemic illness
  • Active gastric ulcer disease
  • Gastroesophageal reflux disease (GERD)

Other

  • Pre-existing nutritional deficiency
  • Pregnancy or lactation
  • Active substance or alcohol abuse
  • Psychologically unstable patients

Who the study is looking for

  • Patients scheduled for laparoscopic sleeve gastrectomy
  • Age between 18 and 60 years at the time of surgery
  • Body mass index (BMI) greater than 35 kg/m2, or greater than 30 kg/m2 with significant obesity-related comorbidity
  • Failure of adequate conservative management, including dietary modification, exercise and/or medical therapy, for at least six months
  • Psychological stability and acceptance of surgical risks

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Kasr Al Ainy Hospital, Faculty of Medicine, Cairo University
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.