To evaluate the efficacy of two drugs methylprednisolone and etoricoxib in laproscopic surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/03/018041
- Lead Sponsor
- Department of anaesthesiology Jln Medical College ajmer
- 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 (20-65 yrs) of either sex
2.ASA physical status I or II
3.Patients scheduled for laparoscopic Surgery under general anaesthesia
Exclusion Criteria
1.ASA Physical Status III or above
2.Patients with impaired kidney or liver functions,
3.A history of drug or alcohol abuse
4.A history of chronic pain or daily intake of analgesics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To evaluate the effect on Post operative Pain. <br/ ><br>2 .To evaluate the effect on PONV.Timepoint: 1. To evaluate the effect on Post operative Pain. <br/ ><br>2 .To evaluate the effect on PONV.
- Secondary Outcome Measures
Name Time Method 1.To assess fentanyl dose consumption. <br/ ><br> 2.To assess duration of analgesia. <br/ ><br> 3.To assess and compare the quality of Post op analgesia <br/ ><br> 4. To assess and compare the hemodynamic changes if any. <br/ ><br> 5. To assess and compare the proportion of patient having adverse <br/ ><br> effects and any other complications. <br/ ><br> 6. To evaluate its effects on PONV, fatigue, sedation.Timepoint: Duration of study is around one year