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. |
|
| 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. |