Incisional Hernia Clinical Trial
Official title:
Non Absorbable Mesh Reinforcement of Midline Incision Closure in High Risk Patients, Onlay Versus Preperitoneal Position, a Comparative Clinical Trial
Verified date | October 2019 |
Source | Zagazig University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
comparison between onlay and preperitoneal augmentation of mid line closure in high risk patients
Status | Completed |
Enrollment | 47 |
Est. completion date | August 2019 |
Est. primary completion date | August 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Obesity - Diabetes mellitus (DM), - Steroid therapy, - Liver diseases, - Renal diseases, - Cardiac diseases, Chest diseases , - Malignancy, - Nutritional deficiency - Old age Exclusion Criteria: - non risk factor - previous incisional hernia |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Zagazig University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | midline incisional hernia , | clinical and ultrasound examination of the abdomen for incisional hernia development | weekly for one month , then monthly for 6 months then every 3 months later on till one year | |
Secondary | post operative complications | hematoma , seroma, wound infection by clinical examination and\or ultrasound | (1st month post operative |
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