Pediatric patient with tonsillectomy
Conditions
Interventions
Group T: The subjects in the group T are received yokukansan suppository (0.25g/kg) during operation.
Group F: The subjects in the group F are injected fentanyl (0.005mg/kg) during operation
Sponsors
Nissay Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: a) Pediatric patient with tonsillectomy under general anesthesia b) Patients that a written informed consent was obtained to participate in this study.
Exclusion criteria
Exclusion criteria: a) Patients who take herbal medicines b) Patients who are allergic to medicines, or foods related to the test material of this trial c) Patients who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial d) Patients who are judged not suitable to participate in this trial by physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of sedation score 0,6 and 12 hours after leaving from operating room between the two groups. Sedation score: Behavioral Observational Pain Scale (BOPS) and Children's Hospital Eastern Ontario Pain Scale (CHEOPS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the Used amount of analgesics between the two groups | — |
Countries
Japan
Contacts
Public ContactRyoko Kawahara
Nissay Hospital Anesthesiology
Outcome results
None listed