To know the effect of using hydroxyethyl starch with lignocaine for reduction of pain that occurs during administartion of propofol
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/053406
- Lead Sponsor
- Dayanand Medical College and Hopsital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients of American Society of Anaesthesiologists(ASA) physical status I and II
18-65 yrs old
either gender
undergoing elective surgery under general anaesthesia
Exclusion Criteria
Emergency surgeries or hemodynamically unstable patients
Patients in whom hand or forearm veins will not be accessible
Uncontrolled hypertensives and diabetic patients
Patients with history of dyspnoea or NYHA III or IV
Patients with elevated serum creatinine
Patient refusal
Known history of allergy to propofol or Hydroxyethyl starch
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of pain on propofol injectionTimepoint: During induction with propofol-pain score wil be assessed every 15 secs till loss of verbal command
- Secondary Outcome Measures
Name Time Method Severity of pain on propofol injection using numerical rating scaleTimepoint: During induction with propofol-pain score wil be assessed every 15 secs till loss of verbal command