Comparison between two mesh groups in open inguinal hernia repair
Phase 2
- Conditions
- Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2022/02/040413
- Lead Sponsor
- Dr Sundeep
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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
- Secondary Outcome Measures
Name Time Method 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