Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: in. propofol {neorof 20ml vial} 200mg: 0.5mg/kg, intravenous
Intervention2: NIL: NIL
Control Intervention1: Injection ketamine: To check the effect of drug on succinyl choline induced p
Sponsors
Dr Akanksha bharat
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA Grade 1,2 2. Age 18 to 65 years 3. Both males and females 4. elective surgeries under general anesthesia with endotracheal intubation under effects of succinyl choline 5. Surgeries completed within 3 hrs
Exclusion criteria
Exclusion criteria: 1. Patient with contraindication to succinyl choline use like chronic deblitating illness, raised intracranial tension, myopathy, recent burns{ 2. Pregnant patients and lactating mothers 3. Patients with severe cardiovascular, liver or renal disease 4. Morbid obesity{BMI >35} 5. Patients with known allergies to the study drug 6. Patients who has received analgesic+ muscle relaxants medication in last 24 hrs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study and compare following parameters in both the groups 1. Severity of fasiculations after succinylcholine administration 2. Incidence of post operative myalgia 3. Severity of post operative myalgia after 24hours and 48 hoursTimepoint: After induction agent for severity of fasiculations, Post operatively 24 and 48 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To study and compare haemodynamic parameters (heart rate and mean arterial pressure) in both groupsTimepoint: Intra operetively 0,2,4,6 minute before induction agent, Intra operatively 0,5,10 minute after intubation | — |
Countries
India
Contacts
Public ContactDr Akanksha Bharat
MGM medical college, aurangabad
Outcome results
None listed