Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: dexamethasone vs ketamine vs lidocaine: Randomization will be done by computer generated random number tables and groups will be assigned by opening sealed sequentially numbered opaque
Sponsors
Department of anaesthesiology AIIMS Rishikesh
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| To assess any complications such as thrombophlebitis, hyperglycemia or any adverse effects of drugsTimepoint: every 10 minutes till end of surgery | — |
Countries
India
Contacts
Public ContactBhavna Gupta
AIIMS, Rishikesh
Outcome results
None listed