Laceration repair.
Conditions
Interventions
Intervention 1: Intervention group: Administering the Ondansetron 1.5 mg/kg (Exir) + Ketamine in sedation. Intervention 2: Control group: Administering the Placebo( normal saline).
Treatment - Drugs
Placebo
Intervention group: Administering the Ondansetron 1.5 mg/kg (Exir) + Ketamine in sedation
Control group: Administering the Placebo( normal saline)
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
1 Years to 1 Years
Inclusion criteria
Inclusion criteria: children aged 1-10 years who received IV or IM ketamine for laceration repair
Exclusion criteria
Exclusion criteria: parents unwilling to provide informed consent history of psychosis , hypertension, intracranial hemorrhage Nothing-by-mouth (NPO) time less than 3 hours use of anti-emetic drugs before treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of nausea and vomiting in the ED. Timepoint: In the emergency department. Method of measurement: The incidence of nausea and vomiting. | — |
Secondary
| Measure | Time frame |
|---|---|
| Other complications of Ketamine and Ondansetron. Timepoint: In the emergency department. Method of measurement: The incidence.;Emergency department length of stay. Timepoint: Before discharge. Method of measurement: Time(minute). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarhad Heydari
Esfahan University of Medical Sciences
Outcome results
None listed