Table 4.
Design | Primary efficacy endpoint | Outcome | Reference |
---|---|---|---|
Single case report, open-label, treatment-resistant schizophrenia, up to 1500 mg/day CBD over 4 weeks | Psychotic symptoms (BPRS; IOSPI) | Improvement in a treatment-resistant patient | Zuardi et al., 1995 |
Open-label, case series (three patients), treatment-resistant schizophrenia, up to 1280 mg/day CBD over 30 days | Psychotic symptoms (BPRS) | One patient showed mild improvement in positive and negative symptoms | Zuardi et al., 2006 |
Double-blind, active controlled acute trial, single CBD (300 or 600 mg) or placebo administration | Stroop Color Word Test (SCWT) | No beneficial effects of single CBD administration on cognitive performance of schizophrenic patients | Hallak et al., 2010 |
Double-blind, active-controlled RCT with 42 acute schizophrenic patients, 600–800 mg/day over 4 weeks | Psychotic symptoms (PANSS/BPRS) | Significant clinical improvement compared to baseline on days 14 and 28 for CBD and amisulpride. Superior side-effect profile for CBD compared to amisulpride | Leweke et al., 2012 |
BPRS, Brief Psychiatric Rating Scale; CBD, cannabidiol; IOSPI, Interactive Observation Scale for Psychiatric Inpatients; PANSS, Positive and Negative Syndrome Scale; RCT, randomized clinical trial.