Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1:
6% Hydroxy ethyl starch: 50 ml of 6% hydroxy ethyl starch will be given intravenously before giving propofol.
Control Intervention1: 0.9% Normal Saline: 50 ml 0.9% Normal saline will
Sponsors
Smt B.K.Shah Medical Institute and Research center
Eligibility
Inclusion criteria
Inclusion criteria: Patient willing to sign the written& informed consent, patients aged between 18 to 60 years belonging to either gender posted for elective surgery under general anaesthesia, patients belonging to American Society of anesthesiologists grade I and II
Exclusion criteria
Exclusion criteria: Patient s refusal from taking part in the study, emergency surgery, patients having history of allergic reaction to propofol or HES, patients with sever cardiorespiratory compromise, diabetes, , raised creatinine level; patients in whom hands or forearm veins are not accessible.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to assess effectiveness of Hydroxy Ethyl starch for reduction of pain on propofol injection.Timepoint: 10 seconds after giving propofol | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Asses severity of pain on propofol injection 2. Asses incidence of pain on propofol injection 3. Asses changes in Heart rate (HR) after Propofol Injection 4. Asses changes in Mean Arterial Pressure (MAP) after Propofol Injection Timepoint: 10 seconds after propofol injection | — |
Countries
India
Contacts
Public ContactDr Jigisha Mehta
Smt B.K. Shah Medical Institute and Research Center, Sumandeep Vidyapeeth deemed to be university,
Outcome results
None listed