Study register · detail
Unclear
GRADE
Moderate
6 citations
Samplen = 29 Pat.
Duration4 weeks treatment + 4 weeks…
ControlPlacebo spray
EndpointCMAI
Blindingdoppelblind
DesignRCT (feasibility study)
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding
Nabiximols showed good tolerability and feasibility, however the recruitment target was not fully reached and efficacy on agitation remains unclear.
Summary
STAND feasibility RCT (n=29) of nabiximols (1:1 THC:CBD) vs. placebo for agitation in Alzheimer's dementia over 4 weeks in UK care homes. Primary goal was feasibility (≥75% follow-up, ≥80% adherence, Cohen's d ≥0,3 on CMAI). Follow-up rate 100%, adherence 100%, no study dropouts, no adverse reactions. Well tolerated and feasible; supports a larger efficacy study.
P
PopulationAdults with probable Alzheimer's dementia and clinically significant agitation in UK care homes, n=29
I
InterventionNabiximols (Sativex®) oromucosal spray (1:1 THC:CBD), 4 weeks up-titrating dosage
C
ControlPlacebo spray
O
OutcomeFeasibility: 29 of 60 targeted participants randomised; 100% adherence; 0% study dropouts; no adverse reactions; effect size on CMAI not reported (Cohen's d ≥0.3 threshold not conclusively assessed)
Confidence in the evidence
Moderate
The third of four GRADE levels, the effect estimate is probably reliable.
Downgraded for
Imprecision
Quality profile
Sample size
★★★★★
Blinding
Double-blind
Effect size
—
Citations / year
★★★★★
Authors
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