Assessment of pain during drug injection when the drug is warm and cold in comparison with warm and cold intravenous fluid
Not Applicable
- Conditions
- Health Condition 1: Z00-Z99- Factors influencing health status and contact with health services
- Registration Number
- CTRI/2019/12/022468
- Lead Sponsor
- MS Ramaiah Medical College and hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients undergoing elective surgeries under general anaesthesia
Exclusion Criteria
Allergy to propofol
Inability to comprehend Verbal Rating Scale (VRS)
Pregnant and breastfeeding women
Peripheral neuropathy
Patients with skin disease or erythema
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the incidence and degree of pain during Propofol injection using warm or cold propofol with heated or cold carrier fluid.Timepoint: immediately after intervention
- Secondary Outcome Measures
Name Time Method To observe hemodynamic changes during propofol injection at different temperatures.Timepoint: baseline, pre-induction, immediately after intervention, every minute for three minutes