A scientific study to compare the two methods of ultrasound guided quadratus lumborum block for post-operative pain reduction in patients coming for unilateral inguinal hernia surgeries.
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/069887
- Lead Sponsor
- Mysore medical College and Research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA I and II patients undergoing unilateral inguinal hernia surgeries
Exclusion Criteria
All ASA III and IV patients.
Patients with comorbid conditions like diabetes, hypertension, cardiovascular, respiratory and neurological disorders, cerebrovascular insufficiency, coagulation abnormalities, renal or hepatic insufficiency.
Obesity.
Drug allergy and allergy to local anesthetics.
Patient refusal for consent.
Infection at the injection site.
Pregnant and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the time taken for first rescue analgesia between 2 approaches of USG guided quadratus lumborum block in patients undergoing unilateral inguinal hernia surgeriesTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method To compare the duration of technique and level of sensory block achieved and total analgesics consumption between 2 approaches of USG guided quadratus lumborum blockTimepoint: 24 hours