Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study wil include 62 patients of either sex of age group 18-60 years, belonging to American Society of Anesthesiologists (ASA) physical status of 1-l posted for elective surgery under general anaesthesia of duration 1-3 hrs.
Exclusion criteria
Exclusion criteria: History of allergy to test drug, History of hepatic and renal dysfunction, History of psychological disorders, History of alcohol and drug abuse, Refusal to participate in the study will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare and study of the effectiveness of two doses of oral paracetamol in alleviating the pain due to propofol injection.Timepoint: inj. propofol 2mgkg-1 given intravenously as total dose. After one fourth of the total dose has been given the assessing anaesthesiologist will use a specially designed composite pain scale described by Rochette and colleagues to evaluate the level of propofol injection pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| To note side effects, if any.Timepoint: 24 hrs. | — |
Countries
India
Contacts
Pt. B D Sharma, PGIMS, Rohtak