To study the patient related outcomes in patient who undergo open method of surgical repair and patients who undergo laparoscopic surgical repair amongst those patients who are suffering from Inguinal Hernia
Not Applicable
- Conditions
- Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2024/08/072358
- Lead Sponsor
- Department of General Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All unilateral inguinal hernias
Exclusion Criteria
Patients with bilateral hernia
Unfit for Surgery
Chronic pain patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient related outcome measures demonstrate better results in patients undergoing Laparoscopic repair for inguinal hernia as compared to open repairTimepoint: 6hrs, 24 hrs, 36 hrs, 72 hrs
- Secondary Outcome Measures
Name Time Method Pain is less in laparoscopic repair as compared to open repair of inguinal herniaTimepoint: 3months