Comparision of 0.25%Ropivacaine versus 0.25%Ropivacaine with Dexmeditomedine in Ultrasound guided Transverse Abdominis Plane Block for Postoperative analgesia in inguinal hernia surgeries.
Phase 4
- Conditions
- Health Condition 1: K40- Inguinal herniaHealth Condition 2: K409- Unilateral inguinal hernia, without obstruction or gangreneHealth Condition 3: K409- Unilateral inguinal hernia, without obstruction or gangreneHealth Condition 4: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2024/03/063850
- Lead Sponsor
- Bangalore 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
American society of Anaesthesiologists (ASA1 and ASA2)
Patients being operated for elective unilateral inguinal hernia under general anaesthesia.
Exclusion Criteria
Patients not willing to give informed consent
Patients with known allergy to any of study drug
Recurrent inguinal hernia patients
Emergency surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess postoperative analgesia using VAS scoreTimepoint: To assess the VAS score at 1,3,6,12,24 hours post operatively.
- Secondary Outcome Measures
Name Time Method Degree of sedation.Timepoint: Degree of sedation using Modified Wilsons score at 1,3,6,12,18,24 hours postoperatively.;Time of first dose of rescue analgesiaTimepoint: Time of requirement of first dose of Tramadol 2mg per kg body weight;To assess Hemodynamic parameters Heart rate and Mean Arterial Pressure post operatively.Timepoint: To assess the Hemodynamic parameters Heart rate and Mean Arterial pressure at 1,3,6,12,18 hours post operatively;Total opiod requirement(Tramadol).Timepoint: Total opioid requirement(Tramadol) in 24 hours.