Methods |
Randomised parallel group |
Participants |
Birth to age of 18 years. |
Interventions |
Arm 1 = midazolam 0.2 mg/kg IM
Arm 2 = diazepam 0.3 mg/kg IV |
Outcomes |
Cessation of seizures
Requirement for ventilatory support
Adverse effects |
Notes |
Study conducted in USA |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
Not described |
Allocation concealment (selection bias) |
Unclear risk |
Not described |
Blinding of participants and personnel (performance bias)
All outcomes |
Unclear risk |
Not described |
Blinding of outcome assessment (detection bias)
All outcomes |
Unclear risk |
Not described |