Propofol injection pain. Pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Study group: Injection of 0.15 micrograms per kilogram immediately before induction of anesthesia Propofol injection 20% . Intervention 2: Control group: Normal Saline at the same volu
Treatment - Drugs
Study group: Injection of 0.15 micrograms per kilogram immediately before induction of anesthesia Propofol injection 20% .
Control group: Normal Saline at the same volume confounding medication immediately before induction of anesthesia Propofol infusion dose by 20%
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
All
Age
6 Years to 13 Years
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Injection site pain, redness, injection site phlebitis. Timepoint: After transferring the patient to recovery. Method of measurement: Visit the site of injection. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHossein Hashemy
Birjand University of Medical Sciences
Outcome results
None listed