Yan 2008.

Methods	Allocation: randomised, no further details. Blindness: unclear. Duration: eight weeks. Design: parallel. Setting: inpatient and outpatient, China.
Participants	Diagnosis: schizophrenia (CCMD‐3). PANSS of 60 or more. N = 60. Age: aripiprazole group: mean = (13. 0 ± 2. 3) years; risperidone group: mean = (13. 0 ± 2. 6) years. Gender: aripiprazole group: 14 male, 16 female; risperidone group: 13 male, 17 female. History: aripiprazole group: mean = (10. 6 ± 6. 0) years; risperidone group: mean = (8. 2 ± 5. 2) years. Age at onset not reported.
Interventions	1. Aripiprazole: Dose range: 2.5‐25 mg/day. Mean dose: not reported. N = 30. 2. Risperidone: Dose range: 0.5‐6 mg/day. Mean dose: not reported. N = 30.
Outcomes	Global state: PANSS score decreased rate (recovery: ≥ 75%, markedly improved: 50%‐75%, improved: 25%‐50%, no effect: < 25%). CGI‐SI score. Mental state: PANSS total score, PANSS positive subscale score, PANSS negative subscale score, PANSS general pathological subscale score. Leaving the study early: no patient. Adverse effects. Unable to use‐ Adverse effects: TESS score, blood routine, hepatorenal function, EEG, and weight (no data).
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	Not reported.
Blinding of participants and personnel (performance bias) All outcomes	Unclear risk	Not reported.
Blinding of outcome assessment (detection bias) All outcomes	Unclear risk	Unclear if outcome was assessed blindly.
Incomplete outcome data (attrition bias) All outcomes	Low risk	No incomplete data.
Selective reporting (reporting bias)	High risk	Although TESS was used to assess adverse effects, no data on scores were available. Data on blood routine, hepatorenal function, EEG, and weight were missing.
Other bias	Low risk	None obvious.