Methods | Allocation: randomly assigned (no further description). Blinding: single, staff ‘remained blind as to whether the patient was receiving medication or placebo’. Duration: unclear; mean hospitalisation=43 days, follow-up at 1-36 months after discharge |
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Participants | Diagnosis: schizophrenia (criteria not specified). N=127. Sex: all male. Age: range 16-40 yrs. History: ‘acute’ illness. |
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Interventions | 1. Chlorpromazine: dose variable 300-900 mg/day. N=53. 2. Placebo. N=74. |
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Outcomes | Leaving study early. Rehospitalisation. Unable to use. Clinical Change Index and Global Assessment Scores (data skewed) |
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Notes | ||
Risk of bias | ||
Bias | Authors’ judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Randomly assigned (no further description). |
Allocation concealment (selection bias) | Unclear risk | No details. |
Blinding (performance bias and detection bias) All outcomes |
Low risk | Reported that “staff remain blind to whether the patient was receiving medication or placebo” |
Incomplete outcome data (attrition bias) All outcomes |
Unclear risk | No details. |
Selective reporting (reporting bias) | Low risk | Differential attrition reported by authors. |
Other bias | Unclear risk | No further details. |