Table 4.
Study | Design/duration | Condition | Sample characteristics | Intervention (No. of patients) | Outcome | Side effects/adverse events | Results | Cochrane risk of bias |
---|---|---|---|---|---|---|---|---|
Alzheimer’s disease | ||||||||
Volicer et al. (1997)22) | Double-blind Crossover | Disturbed behavior in Alzheimer’s disease |
|
|
|
Common side effects:
|
|
Unclear |
Dementia | ||||||||
Walther et al. (2011)23) | Crossover | Nighttime agitation in Alzheimer’s disease |
|
|
|
No adverse event |
|
Unclear |
van den Elsen et al. (2015)24) | Double-blind Crossover | Dementia |
|
|
|
Common side effects:
|
|
Unclear |
van den Elsen et al. (2015)25) | Double-blind Crossover | Dementia |
|
|
|
Lack of information on common adverse event |
|
Unclear |
Amyotrophic lateral sclerosis (ALS) | ||||||||
Weber et al. (2010)26) | Double-blind Crossover | ALS |
|
|
Primary:
|
2 serious adverse events |
|
Unclear |
CMAI, Cohen-Mansfield Agitation Inventory; NPI, Neuropsychiatric Inventory; THC, tetrahydrocannabinol; QoL-AD, Quality of Life in Alzheimer’s Disease scale; CCGIC, Caregiver Clinical Global Impression of Change; ZBI, Zarit Burden Interview; VAS, visual analogue scale; ALSFRS-R, ALS functional rating scale revised; ALSAQ-40, ALS assessment questionnaire; SDQ24, Sleep Disorder Questionnaire.
• Total (completed)/• male:female/• age.