None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adult patients aged 18 65 years. 2. Patients diagnosed with primary unilateral or bilateral inguinal hernia. 3. Patients planned for elective Lichtenstein tension-free hernioplasty. 4. Patients who are fit for surgery under spinal or general anesthesia. 5. Patients who are willing to participate and able to provide written informed consent.
Exclusion criteria
Exclusion criteria: 1. Recurrent inguinal hernia. 2. Complicated hernias (strangulated, obstructed, incarcerated). 3. Femoral hernia or other types of groin hernias. 4. Patients requiring emergency surgery. 5. Patients with severe comorbidities (e.g., uncontrolled diabetes, severe cardiac or pulmonary disease) that increase surgical risk. 6. Known allergy or sensitivity to cyanoacrylate glue. 7. Patients with immunocompromised conditions. 8. Patients unwilling or unable to provide informed consent. 9. Pregnant or lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative pain assessed using the Visual Analogue Scale (VAS). Timepoint: Baseline (pre-operative) 4 weeks post-operative 8 weeks post-operative | — |
Secondary
| Measure | Time frame |
|---|---|
| seroma hematoma wound infection chronic groin painTimepoint: week, 1 month, 3 month | — |
Countries
India
Contacts
Professor