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NCT06209450 Clinical Trial

Sutured vs Sutureless Mesh Fixation for Onlay Ventral Hernia Repair

Ventral Hernia Clinical Trial

Official title:
Sutured vs Suturless Mesh Fixation for Onlay Ventral Hernia Repair

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06209450
Other study ID # Hernia
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2024
Est. completion date March 1, 2025

Study information
Verified date January 2024
Source Assiut University
Contact Khaled Muhammad Mahmoud
Phone 01069094017
Email Khaledgad19844@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison beta sutured and suturless mesh fixation for ventral hernia regarding recurrence rates and complications rate

Description:

Ventral hernia repair is common procedure with over 250000 repairs each year in the unites states . Most ventral hernias are repaired using tension free type of repair using mesh that bridge the defect and reinforce the abdominal wall . The mesh fixation technique has impact on recurrence rates,chronic pain and complications rates . Suturless ventral hernia repair with sealing agent fixation proved to be durable with comperable complication profile to other techniques.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 1
Est. completion date March 1, 2025
Est. primary completion date March 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - ventral hernia - both sexes Exclusion Criteria: - obstructed or complicated ventral hernia - incisional hernia - recurrent hernia - multiple ventral hernia - large hernia more than 5 cm

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Ventral hernia repair with mesh fixation
Sutured versus suturless mesh fixation

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary Complications Intraoperative and post operative complications occur due to technique used in study One year after surgery
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