Pain of Propofol Intravenous Injectio
Not Applicable
- Conditions
- pain.Pain in limb
- Registration Number
- IRCT2016051410340N10
- Lead Sponsor
- Golestan University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
people aged 18-65 years that categorized into class 1 and 2 based on America Society of Anesthesiologists (ASA); hypertension between 90 and 140 until 24 hours before surgery; lack of neurological disorders, kidney and liver failure; lack of drug allergy; no history of allergy to eggs or anaphylaxis.
Exclusion criteria were considered as: having allergies or symptoms of heart disease and arrhythmias; saturation drops below 90%; operation duration more than 3 hours.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: After intervention. Method of measurement: Verbal Rating Scale.
- Secondary Outcome Measures
Name Time Method Hemodynamic Change. Timepoint: Before Intervention, 1,3 and 5 minutes after intervention. Method of measurement: Sphygmomanometer, Pols oximeter.