Comparision of two different meshes in Hernia repair surgery
Phase 2
- Conditions
- Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2019/12/022498
- Lead Sponsor
- Dr Ajaypandian
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients of age above 18 years with unilateral inguinal hernia presenting to PIMS undergoing surgery, willing to participate in this study
Exclusion Criteria
1.Patients with strangulated hernia,
2.Recurrent hernia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the postoperative pain following Lichtenstein inguinal hernioplasty using polyester vs. polypropylene meshTimepoint: Post operatively after 1 week and after 3 months
- Secondary Outcome Measures
Name Time Method 1. Assessment of inflammatory markers like [hsCRP, IL 6] in pre-op and postop at 12 hours <br/ ><br>2.To document the duration of operative time, duration of hospital stay. <br/ ><br>3.Assessment of surgical site infections, seroma and hematoma formationTimepoint: Post operative assessment