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Prophylactic Mesh Reinforcement for Stoma Closure

NCT06157645 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2025-12-15

No results posted yet for this study

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

Conditions

  • Incisional Hernia
  • Surgical Site Infection
  • Postoperative Pain
  • Hospital Stay, Length of Stay in Hospital From Surgery to Discharge
  • Complication

Interventions

DEVICE

Prolene mesh

Application of mesh onlay post stoma closure

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Principal Investigators

  • Mostafa Thabet, Professor · Assiut University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-01
Primary Completion
2025-07-01
Completion
2025-09-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06157645 on ClinicalTrials.gov