Assessment of postoperative pain relief in patients coming for laparoscopic abdomen surgeries using two different drugs under ultrasound guidance
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064042
- Lead Sponsor
- Sree Balaji Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted all laparoscopic surgeries
ASA grade 1 and ASA grade 2
patient who are willing to participate
Exclusion Criteria
ASA grade 3 and ASA grade 4
Patients who are known case of hypersensitivity to amide group of local anesthetic agents
Patients with coagulation disorders
patient who are not willing to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe the duration of analgesia between the two different study groupsTimepoint: by observing hourly VAS score
- Secondary Outcome Measures
Name Time Method To find out the time of first rescue analgesiaTimepoint: To find out the Pain score at 4hr 8hr 12hr 18hr and 24hr postoperatively