It is the study done in spinal surgeries after completion of surgery. It is to assess the pain and sedation in post operative period for 24 hours .the study is to compare between two drugs

Phase 3

Not yet recruiting

• Conditions: Health Condition 1: 8- Other Procedures

• Registration Number: CTRI/2022/07/044302
• Lead Sponsor: nil

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2 August 2022

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients with American Society Of Anaesthesiologists Grade 1 and 2

patients with normal pulmonary function tests

patients undergoing spine surgeries

Exclusion Criteria

patients with American Society Of Anaesthesiologists 3 and 4

patients on any opoids or any sedative medication in the week prior to the surgery

patients with history of alcohol or drug abuse

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1) vitals in post operative period <br/ ><br>2) scoring of pain <br/ ><br>3) sedation score <br/ ><br>4) Any side effects in post operative periodTimepoint: From time of completion of surgical procedure till 24hours postoperatively

Secondary Outcome Measures

Name	Time	Method
1) Any side effects in post operative period in spine surgeries <br/ ><br>Nausea, vomitingTimepoint: till 24 hours postoperatively