A Randomized Trial Comparing Pain-related Outcomes Using Objective Pain Measurement Following Laparoscopic And Open Groin Hernia Repair
Not Applicable
- Conditions
- Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangreneHealth Condition 2: O- Medical and SurgicalHealth Condition 3: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2022/09/045456
- Lead Sponsor
- Dr Jasmine Dhal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients with uncomplicated primary groin hernia, fit to undergo either laparoscopic groin hernia repair or Lichtenstein open mesh repair
Exclusion Criteria
1. Age < 18 years or > 75 years
2. Complicated, i.e., strangulated or obstructed hernia
3. Recurrent inguinal hernia
4. History of previous pelvic or lower abdominal surgery
5. History of hernia repair either on same or contralateral ide
6. History of chronic systemic or mental illness
7. Diabetes mellitus and chronic kidney disease
8. Chronic analgesic/ opioid abuse
9. Unfit for general anesthesia
10. Coagulopathies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method