Respiratory disease, acute respiratory failure, poisoning by drugs and medications, acute pain, allergies, digestive disorders
Conditions
Interventions
This study consists of two arms: placebo and intervention. Patients in the intervention group receiving ketamine drug dose 4 mg / kg once, and those in the placebo group received saline at a dose 4 mg
Drug
D26.660
Sponsors
Hospital de Clínicas de Porto Alegre
Hospital de Clínicas de Porto Alegre
Eligibility
Age
3 Months to 12 Years
Inclusion criteria
Inclusion criteria: Children hospitalized in the Pediatric Inpatient Units, with the presence of legal guardian; aged 3 months to 12 years; requiring venipuncture independent research.
Exclusion criteria
Exclusion criteria: Severe neurological sequelae; Patients who need immediate venipuncture at risk; Presence of active nosebleeds; Patients using antipsicotrópicos; Children who have experienced clinical change with ketamine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Decreased venipuncture time in sedated patients with a variation of 3 and a difference of 3 minutes compared to patients not sedated, checked by timing the venipuncture time | — |
Secondary
| Measure | Time frame |
|---|---|
| Easier implementation of venipuncture performed by nurses using a questionnaire as a tool | — |
Countries
Brazil
Contacts
Public ContactSabrina Pinheiro
Hospital de Clínicas de Porto Alegre
Outcome results
None listed