Akhondzadeh 2005.
Methods | Allocation: randomised. Blindness: double‐blind. Duration: 8 weeks. Setting: hospital, Iran. Design: parallel groups. | |
Participants | Diagnosis: schizophrenia (DSM‐IV) and PANSS > 59 criteria). N = 46. Sex: 13 female, 33 male. Age: average 33.8 (selegiline), 35.0 (placebo) | |
Interventions | 1. Allopurinol: 300mg. N = 23. 2. Placebo. N = 23. Stable neuroleptic medication: haloperidol 15 mg. | |
Outcomes | Leaving the study early. Mental state: PANSS change score. Adverse events: various specific effects. |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated. |
Allocation concealment (selection bias) | Unclear risk | No further details. |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Double‐blind. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No further details. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | LOCF analysis reported. |
Selective reporting (reporting bias) | Low risk | Main outcomes reported. |
Other bias | Low risk | None obvious. |