A comparative study of 0.375% Ropivacaine versus 0.25% Bupivacaine for post operative pain relief following upper abdominal surgeries using ultrasound guided transversus abdominis plane block
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052181
- Lead Sponsor
- Department of anesthesia ABVIMS AND DR RML HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Adult patients in the age group 18 to 60 years (BMI 18-30kg/m2) 2. Undergoing elective upper abdominal surgery under standard general anaesthesia.
3. ASA Grade I and II patients.
Exclusion Criteria
Pregnant Women
Allergy to opioids, amide group of local anaesthetics and non-steroidal antiinflammatory drugs
Coagulopathy or bleeding disorder.
Infection at block site.
Patients with cardiovascular, pulmonary or neurological diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method