Comparison of two drugs at surgical site infiltration in patients undergoing lumbar spine surgery
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/12/060677
- Lead Sponsor
- SMS Medical College And Attached Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients willing to give written informed
consent.
2. Patient undergoing Lumbar spine surgery.
Patients of either gender with age group
ranging from 25 to 60 years.
3. ASA grade I and II.
Exclusion Criteria
1. History of seizure, severe systemic disease,
mental illness, renal dysfunction, , history of
peptic ulcer disease and antacid therapy,
coagulopathy, and drug abuse.
2. History of allergy to any of the drugs used
during the study.
3. BMI > 35 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Mean VAS score. <br/ ><br>2. Mean duration of post <br/ ><br> operative analgesia. <br/ ><br>3. Mean number & total doses <br/ ><br> of rescue analgesia <br/ ><br> required in 24hours. <br/ ><br>4. Mean post operative <br/ ><br> hemodynamic parameters (HR, <br/ ><br> SBP, DBP, MBP). <br/ ><br> <br/ ><br>Timepoint: 0 HOUR <br/ ><br>6 HOUR <br/ ><br>12 HOUR <br/ ><br>24 HOUR <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Proportion of cases with <br/ ><br> side effects. <br/ ><br>Timepoint: 24 HOURS