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Non Absorbable Mesh Reinforcement of Midline Incision Closure in High Risk Patients, Onlay Versus Preperitoneal Position, a Comparative Clinical Trial

NCT04145908 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2019-10-31

No results posted yet for this study

Summary

comparison between onlay and preperitoneal augmentation of mid line closure in high risk patients

Conditions

  • Midline Incisions
  • High Risk Patients
  • Mesh Reinforcement
  • Incisional Hernia

Interventions

PROCEDURE

midline mesh reinforcement

augmentation of midline closure by nonabsorbsble mesh

Sponsors & Collaborators

  • Zagazig University

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2019-08-31
Completion
2019-08-31

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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 NCT04145908 on ClinicalTrials.gov