Effect of Dexamethasone to prevent Propofol injection pai
Not Applicable
- Conditions
- Propofol injection pain.Pain, not elsewhere classified
- Registration Number
- IRCT2016011325992N1
- Lead Sponsor
- Birjand University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Children ages 6 to 13 years undergoing elective surgery (tonsillectomy, adenotonsillectomy, adenoctomy, lower extremity fractures).
Exclusion criteria: included children crying when entering the operating room; emergency; abnormal liver and renal function; musculoskeletal disorders and allergy to Propofol, Dexamethasone; and also entering an intravenous line in the back of their hand are impossible.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Facial expressions child. Timepoint: Immediatly after the injection 20% of the doss of Propofol anesthesia. Method of measurement: Face Pain Scale (FPS) with rating (0 to 10).;Heart rate of patient. Timepoint: Before Dexamethasone and Normal Saline injection and after administration of anesthesia Propofol dose by 20%. Method of measurement: In bits per minute using ECG.
- Secondary Outcome Measures
Name Time Method Injection site pain, redness, injection site phlebitis. Timepoint: After transferring the patient to recovery. Method of measurement: Visit the site of injection.