Tonsillectomy. Acute tonsillitis, unspecified
Conditions
Interventions
Intervention 1: Intervention group (G) : In all three groups, after the induction of anesthesia, the patients receive intravenous drugs of the studied analgesic regimen, which includes 500 µg/kg of ke
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
4 Years to 10 Years
Inclusion criteria
Inclusion criteria: Patients with ASA grade I or II (American Society of Anesthesiology classification) Patients between 4 and 10 years old Candidate for tonsillectomy or adenotonsillectomy with diagnosis of tonsillitis The distance between the hospital and the patient's place of residence should be a maximum of 30 minutes by car
Exclusion criteria
Exclusion criteria: Allergy to the drugs used in the study Positive history of liver, kidney, Coagulation disorders and Diseases of the digestive system Positive history of uncontrolled diseases of the cardiovascular system Obstructive sleep apnoea Taking painkillers other than study drugs in 24 hours before surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Every 15 minutes in the recovery room and at 24, 12, 6, 4, 2 hours after surgery. Method of measurement: CHEOPS scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| The quality of the patient's sleep. Timepoint: First time. Method of measurement: In respect to standardized questionnaire.;Painless swallowing. Timepoint: First time. Method of measurement: Patient history taking.;The level of satisfaction of the patient's parents. Timepoint: After recovery. Method of measurement: In respect to standardized questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Nemati
Shiraz University of Medical Sciences
Outcome results
None listed