Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:52 AM
Ignite Modification Date:
2025-12-25 @ 2:52 AM
NCT ID:
NCT02387333
Eligibility Criteria:
Inclusion Criteria:
1. Ability to give informed consent.
2. Patients with history of chronic liver disease
3. Patients with history of systemic chemotherapy, radiotherapy or maintenance on systemic corticosteroids
4. Patients with chronic causes of increased intra-abdominal pressure as chronic cough (COPD) or chronic constipation
5. Patients with surgical history of hernia repair
6. Patients with body mass index (BMI) more than 30 kg/m2
7. Patients with other hernias (inguinal, umbilical or incisional) at preoperative evaluation
8. Patients with low serum albumin \< 3 gm/dl
9. Patients who will be highly candidates for adjuvant or palliative chemo-radiotherapy such those with histopathologically proved residual tumor
Exclusion Criteria:
1. Inability to give informed consent.
2. Patients who documented previous allergic reaction to synthetic mesh.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02387333
Study Brief:
Protocol Section:
NCT02387333