Methods |
Randomised double‐blind placebo‐controlled trial |
Participants |
Depressed inpatients aged 6‐12 years
Gender unknown
13 active treatment, 14 placebo
4 withdrawals |
Interventions |
Imipramine. Dose not stated |
Outcomes |
Children's Depression Rating Scale
Follow‐up interval 6 weeks |
Notes |
Study quality score = 18 |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
High risk |
Not stated |
Allocation concealment (selection bias) |
High risk |
|
Blinding (performance bias and detection bias)
of participants |
Unclear risk |
No description was provided |
Blinding (performance bias and detection bias)
of personnel |
Unclear risk |
No description was provided |
Blinding (performance bias and detection bias)
of outcome assessors |
Unclear risk |
No description was provided |
Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
Numbers and reasons for withdrawals were provided but analysis was not modified |
Selective reporting (reporting bias) |
Unclear risk |
‐ |
Other bias |
Unclear risk |
Previous or concurrent treatments were not stated |