Sun 2000.
Methods | Allocation: randomised. Blindness: not described. Duration: 6 weeks. Setting:no details. |
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Participants | Diagnosis: schizophrenia CCMD‐2‐R. N = 103. Age: mean 31 ± 9 years. Sex: male and female, History: length of illness not stated. Included: not stated. Excluded: not stated. Consent: not stated. |
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Interventions | 1. Perphenazine: 8‐60 mg/day, n = 51. 2. Clozapine: 50‐600 mg/day, n = 51. 3. Perphenazine + clozapine: 32‐50 mg/day + 100‐300 mg/day, n = 51. |
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Outcomes | Curative effect (improvement: cured = psychiatric symptoms disappeared, insight recovered, BPRS reduction >80%; markedly improved = majority of symptoms disappear, some insight, BPRS reduction > 60% to 79%; improvement = some psychiatric symptoms disappeared, no insight, BPRS reduction > 30% to 59%; no effect = no change/ worse symptoms, BPRS reduction < 30%. BPRS, TESS score, adverse events. |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Randomised – no further details. |
Allocation concealment (selection bias) | Unclear risk | No details. |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | No details. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | No details. |
Selective reporting (reporting bias) | Unclear risk | No details. |
Other bias | Unclear risk | No details as to blinding; two raters involved in administering BPRS and TESS. |