Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Intervention1: polyester mesh
polypropylene mesh: litchtenstein tension free repair
Intervention2: lichtenstein tension free repair: Open inguinal hernioplasty- with placement of either one of two mes
Sponsors
Dr Sundeep
Eligibility
Inclusion criteria
Inclusion criteria: Patients of both sexes aged more than 18 years of age and giving valid written informed consent. Patient with unilateral or bilateral inguinal hernia
Exclusion criteria
Exclusion criteria: Complicated hernia Co-morbidities Recurrent inguinal hernia COPD/BPH or any other associated illness causing increased intra-abdominal pressure Patients not willing for the study
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| to assess the complication rate among both mesh group like seroma, infectionTimepoint: to assess the complication rate among both mesh group like seroma, infection at 24 hours, 48 hours, 1 week, 3 weeks, 3 months | — |
Primary
| Measure | Time frame |
|---|---|
| To assess the post operative pain between polypropylene mesh and polyester meshTimepoint: Post operative pain is assessed 24 hours, 48 hours, 3 days, 7 days, 2 weeks, 4 weeks , 3 months using visual analogue scale | — |
Countries
India
Contacts
Public ContactDrTharun Ganapathy
Srm Medical College Hospital and Research Centre
Outcome results
None listed