A clinical trial to study the combined effect of two blocks on post-operative analgesia in patients undergoing laparascopic abdominal surgeries.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/09/045500
- Lead Sponsor
- PRIYANGA A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA 1 and 2
2. Elective and Emergency laparascopic cholecystectomy
3. BMI less than 30
Exclusion Criteria
1. Open abdominal surgeries
2. Coagulation disorders
3. Local infection at the site of injection
4. Patient refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia between two different blocksTimepoint: 0 mins (At the start of surgery), Every 5 minutes for the first 30 minutes of the surgery, Every 10 minutes for the next 30 minutes of the surgery, Every 15 minutes for the next 30 mins of the surgery, and every hour after arrival at PAC
- Secondary Outcome Measures
Name Time Method