Skip to main content
. 2014 Jan 2;2014(1):CD006569. doi: 10.1002/14651858.CD006569.pub5

Tao 2008.

Methods Allocation: randomised, no further details.
 Blindness: unclear.
 Duration: eight weeks.
 Design: four arms intervention.
 Location: inpatient, China.
Participants Diagnosis: schizophrenia (CCMD‐3). PANSS of 70 or more.
 N = 360.
 Age: aripiprazole group: mean = (30. 72 ± 11. 59) years; risperidone group: mean = (32. 51 ± 14. 30) years; quetiapine group: mean = (35. 53 ± 14. 23) years; ziprasidone group: mean = (26. 03 ± 7. 23) years.
 Gender: aripiprazole group: 22 male, 68 female; risperidone group: 43 male, 47 female; quetiapine group: 4 male, 86 female; ziprasidone group: 65 male, 25 female.
 History: not reported. Age at onset not reported.
Interventions 1. Aripiprazole: Dose range: 10‐30 mg/day. Mean dose:not reported. N = 90.
 2. Risperidone: Dose range: 2‐5 mg/day. Mean dose:not reported. N = 90.
3.Quetiapine: Dose range: 200‐600 mg/day. Mean dose:not reported. N = 90.
4.Ziprasidone: Dose range: 40‐80 mg/day. Mean dose:not reported. N = 90.
Outcomes Global state: PANSS score decreased rate (recovery: ≥ 80%, markedly improved: 50%‐80%, improved: 25%‐50%, no effect: < 25%).
Mental state: PANSS total score. PANSS positive subscale score, PANSS negative subscale score, PANSS general pathological subscale score.
Leaving the study early.
Adverse effects.
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 The total rate of loss to follow‐up was 4.4%(3/90 vs. 1/90), 1 participant dropped out because of adverse effect, 1 dropped out because of no effect, 2 dropped out because of incomplete data.
Selective reporting (reporting bias) Low risk No selective reporting.
Other bias Low risk None obvious.