At a glance
ClinicalIndex Comparison RecordN/ACompleted· 62 enrolled
Drug / intervention
Prolene meshdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prophylactic Onlay Mesh Reinforcement vs Anatomical Closure in Stoma Reversal: A Randomized Controlled Trial
In Brief
A clinical study evaluating Prolene mesh for Incisional Hernia and 4 related conditions. Completed, enrolled 62 participants across 1 site.
Detailed Summary
In the current work we are aiming to compare between the mesh-reinforced stoma closure and the anatomical closure in terms of the risk of developing surgical site incisional hernia (SSIH),incidence of surgical site infection , post-operative Pain and Hospital stay
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIncisional Hernia, Surgical Site Infection, Postoperative Pain, Hospital Stay, Length of Stay in Hospital From Surgery to Discharge, Complication
CountriesEgypt
Collaborators--
Timeline
N/ACompletedFinished
202420252026
First PostedDec 2023
Enrollment StartSep 2024
Primary CompletionJul 2025
Study CompletionSep 2025
TodayJul 2026
First PostedDec 6, 2023
Enrollment StartSep 1, 2024
Primary CompletionJul 1, 2025
Study CompletionSep 1, 2025
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 2.6 years ago
Interventions
Prolene meshdevice
Application of mesh onlay post stoma closure