To predict an effective method to reduce propofol injection pain during induction of anaesthesia.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/12/048374
- Lead Sponsor
- Dr Maria Tresa Alex
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 AND 2 PATIENTS UNDERGOING ELECTIVE UNDER GENERAL ANESTHESIA
Exclusion Criteria
EMERGENCY SURGERY
KNOWN HISTORY OF ALLERGY TO PROPOFOL OR HES
PRESENCE OF LEFT VENTRICULAR DYSFUNCTION
PREGNANCY
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the incidence of pain on propofol injection in patients receiving 6% Hydroxyethyl starch bolus prior to propofol, cold propofol and propofol at room temperature.Timepoint: The incidence of pain will be assessed every 5seconds from the time injection till loss of verbal contact
- Secondary Outcome Measures
Name Time Method To compare the severity of propofol injection pain and hemodynamic responseTimepoint: Every 5 seconds till loss of verbal contact