Comparison of three drugs in reduction of pain because of anaesthetic drug.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/02/023522
- Lead Sponsor
- Department of anaesthesiology AIIMS Rishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
The study will include patients belonging to ASA I, age group of 18 to 65 years, weighing 40-80 kg, receiving general anesthesia for elective surgery
Exclusion Criteria
Patients with known hypersensitivity to either lignocaine or dexamethasone or ketamine or propofol or egg or soyabean oil.
Patients with a history of central nervous system or neuro-muscular disease or
psychiatric illness.
Patients with history of drug or alcohol abuse.
History of chronic pain, or taking analgesics or sedatives preoperatively.
Pregnant and lactating females.
Patients with difficult venous access and small caliber veins.
Patients requiring rapid sequence induction
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To assess reduction in propofol induced pain by verbal rating score among groups pretreated with ketamine, dexamethasone and lignocaineTimepoint: every 30 seconds after giving propofol injection till patient is induced
- Secondary Outcome Measures
Name Time Method To assess any complications such as thrombophlebitis, hyperglycemia or any adverse effects of drugsTimepoint: every 10 minutes till end of surgery