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. |
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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 Unable to use ‐ Mental state: BPRS (no SD), Keio University Psychiatric Rating Scale (unpublished scale). |
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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. |