A Clinical Study to find effectiveness of Block performed using Ultrasound in Back of Abdomen for pain relief after surgery in patients undergoing Laparoscopic Kidney Surgeries
Not Applicable
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2019/01/017254
- Lead Sponsor
- SRM medical College Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Patients with ASA Physical Status I and II posted for unilateral laparoscopic renal and hernia surgeries
2. Weighing between 60 â?? 100 kg
3. Age group of 18 â?? 60 year
Exclusion Criteria
1. All patients with ASA Physical Status III and above
2. Patients who refuse to participate in the study
3. Patients who are allergic to amide local anaesthetics
4. Patients who are pregnant
5. Patients with chronic cardiac or hepatic condition
6. Patients with coagulation abnormalities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesiaTimepoint: 24 hours after block
- Secondary Outcome Measures
Name Time Method Consumption of analgesicsTimepoint: For 24 hours after block