Closure Versus Non-Closure of Working Ports in Laparoscopic Sleeve Gastrectomy
NCT07919067, Not applicable, Completed, Kasr El Aini Hospital
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Closure Versus Non-Closure of Working Ports in Laparoscopic Sleeve Gastrectomy | ClinicalTrials.gov |
| NCT number | NCT07919067 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 160 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Kasr El Aini Hospital | ClinicalTrials.gov |
| Conditions | Severe Obesity, Port-Site Hernia, Postoperative Pain | ClinicalTrials.gov |
| Interventions | Non-closure of working port fascia (skin closure only), Fascial closure of working ports | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Incidence of port-site hernia | 12 months after surgery | Number and percentage of patients who developed a port-site (trocar-site) hernia at the working port sites. Diagnosis was based on clinical examination at each follow-up visit (presence of swelling at the trocar site) with radiological confirmation by abdominal wall ultrasound at 1 year. | ClinicalTrials.gov |
| Secondary | Postoperative port-site pain (Visual Analogue Scale) | 1 week and 1 month after surgery | Port-site pain assessed with the Visual Analogue Scale (VAS), range 0 (no pain) to 10 (worst possible pain); higher scores indicate worse pain. Mild pain = 1-3, moderate pain = 4-7, severe pain = 8-10. Clinically significant pain is defined as VAS 4 or more; the number of patients with clinically significant pain is reported in each group. | ClinicalTrials.gov |
| Secondary | Functional recovery (Quality of Recovery-15 score) | 1 week after surgery | Quality of postoperative recovery assessed with the 15-item Quality of Recovery (QoR-15) questionnaire, covering physical well-being, pain and emotional state. Total score ranges from 0 to 150; higher scores indicate better recovery. Scores are categorized as excellent (136-150), good (122-135) or moderate (90-121); the percentage of patients with excellent recovery is reported in each group. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)