Check efficacy of intravenous lidocaine for analgesia in post operative period.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/09/027564
- Lead Sponsor
- INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES
- 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 PARTICIPATE.
2.PATIENTS OF ASA I AND II.
3.PATIENTS SCHEDULED TO UNDERGO ELECTIVE SURGERY.
Exclusion Criteria
1. PATIENTS REFUSAL TO PARTICIPATE.
2. PATIENTS WITH KNOWN TO HYPERSENSITIVITY.
3. PATIENTS IN WHOM LIDOCAINE IS CONTRAINDICATED.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO ASSESS PAIN TROUGH THE VISUAL ANALOGUE SCALETimepoint: 2 HOURLY FOR 6 HOURS AND THEN 6 HOURLY TILL 24 HOUR
- Secondary Outcome Measures
Name Time Method TO STUDY REQUIREMENT OF POST OPERATIVE OPIOD CONSUMPTIONTimepoint: 2 HOURLY FOR 6 HOURS AND THEN 6 HOURLY TILL 24 HOUR