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NCT05005663 Clinical Trial

Incisional Hernia in Infants and Children

Incisional Hernia Clinical Trial

Official title:
Incisional Hernia in Children and and Infants : a Tertiary Center Experience

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05005663
Other study ID # 34687/5/21
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 2, 2007
Est. completion date January 22, 2023

Study information
Verified date April 2022
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the study of development of incisional hernia in infants and children at a tertiary level experience.

Description:

Background: incisional hernia in children and infants (IHCI) represents a major complication following exploration. The condition is associated with prolonged hospital stay, readmission and the need for another operation to treat the resulting incisional hernia. The incidence is variable worldwide. The leading causes are still indeterminate as well as the management strategy. We aimed at studying IHCI at a tertiary level hospital as regard presenting symptoms, methods of management and its impact on the quality of life of patients. Methods: a retrospective study included all infants and children presented with incisional hernia. Patients were categorized in to two groups according to the age of presentation, group A patients younger than two years of age and group B patients older than two years. All data related to the first operation in addition to data related to repair of the incisional hernia were collected in special charts.

Recruitment information / eligibility
Status Recruiting
Enrollment 67
Est. completion date January 22, 2023
Est. primary completion date December 20, 2022
Accepts healthy volunteers No
Gender All
Age group 8 Months to 18 Years
Eligibility Inclusion Criteria: - all infants and children with incisional hernia Exclusion Criteria: - congenital abdominal wall defects

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• surgical management of incisional hernia
surgical repair of the incisional hernia

Locations
Country Name City State
Egypt Faculty of Medicine Tanta

Sponsors (1)
Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary repair of incisional hernia surgical repair 2 years
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