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. 2015 Mar 6;2015(3):CD003443. doi: 10.1002/14651858.CD003443.pub3

Itoh 1976.

Methods Allocation: randomised.
 Blindness: double.
 Duration: 12 weeks, preceded by one week wash‐out.
 Setting: multi‐centre, Japan.
Participants Diagnosis: schizophrenia (hebephrenia (n = 74), catatonia (n = 5), paranoid (n = 18) undifferentiated (n = 8)).
 N = 105.
 Age: range 19 to 50.
 Sex: 58 F, 47 M.
 History: inpatient; duration of hospitalisation of less than one year (n = 32), one to five years (n = 29), five years plus (n = 44); duration of illness range from less than one year to 10 years.
Included: not clear.
 Excluded: somatic diseases; allergy; history of side effects of antiparkinsonians; glaucoma; prostate‐hypertrophy; children; pregnancy and older patients.
Consent: not clear.
Interventions 1. Perphenazine: one tablet (a 4 mg) three times daily for the first week, 2 tablets three times daily in the second week, 3 tablets three times daily in the third week, then flexible dose according to the judgement of each physician; maximum 60 mg daily, n = 51.
 2. Penfluridol: 1 tablet (a 20 mg) daily for the first week, 6 tablets in the second week, 9 tablets in the third week, then flexible dose according to the judgement of each physician; maximum 100 mg daily, n = 54.
Outcomes Leaving the study early.
 Global state: no better or worse.
 Adverse events.
Unable to use ‐ 
 Mental state: BPRS (no SD), Keio University Psychiatric Rating Scale (unpublished scale).
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 clear.
Blinding (performance bias and detection bias) 
 All outcomes Unclear risk Double‐blind: no further details.
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk Not clear.
Selective reporting (reporting bias) Unclear risk Not clear.
Other bias Unclear risk Funding: not clear.
Raters: not stated to be independent of treatment.