Study | Reason for exclusion |
---|---|
Akimoto 1966 | Method: randomised. Participants: chronic schizophrenic participants. Intervention: perphenazine versus placebo. |
Anon 2006 | Method: randomised. Participants: schizophrenic participants. Intervention: perphenazine versus atypical antipsychotics. |
Bennett 1961 | Method: randomised. Participants: schizophrenia. Intervention: perphenazine, chlorpromazine. Outcome: no usable data. |
Casey 1960 | Method: randomised. Participants: schizophrenia. Intervention: perphenazine, chlorpromazine. Outcome: no usable data. |
Hollister 1974 | Method: not randomised. |
Lapolla 1967 | Method: randomised. Participants: hospitalised schizophrenic participants. Intervention: perphenazine in combination with amitriptyline versus chlorpromazine alone. |
Loza 2001 | Method: randomised. Participants: schizophrenic participants. Intervention: perphenazine versus atypical antipsychotics. |
Nordic 1986 | Method: randomised. Participants: psychiatric participants with tardive dyskinesia, not exclusively people with schizophrenia, how many participants had schizophrenia or related disorders was not reported. |
Schulsinger 1958 | Method: not randomised. |
Smith 1959 | Method: not randomised. |
Svestka 1972 | Method: not randomised. |
Svestka 1974 | Method: not randomised, but double‐blind. Cross‐over study, results of first phase not reported separately. Participants: acute exacerbation of psychosis (mainly schizophrenia) Intervention: perphenazine versus oxypertine (difficult to classify, probably a mid‐potency antipsychotic). |
Vinar 1968 | Method: randomised. Participants: schizophrenia. Intervention: perphenazine, chlorpromazine, levomepromazine, thioridazine. Outcome: no usable data, only total number of participants leaving early (no data for single drugs), no rating scale results (no mean, no SD). |
SD ‐ standard deviation