Intravenous colloid infusions for prevention of pain on propofol injectio
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/05/025000
- Lead Sponsor
- Dr Satyajeet Misra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 128
Inclusion Criteria
ASA I and II patients undergoing elective surgery under general anaesthesia
Exclusion Criteria
Hypertensives; diabetics; known LV dysfunction; known allergy to Propofol or hydroxyethyl starch
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain on propofol injectionTimepoint: During administration of propofol while giving anesthesia
- Secondary Outcome Measures
Name Time Method Patient satisfactionTimepoint: 2 hours after recovery from anesthesia