Study register · detail
Clear benefit
GRADE
Moderate
11 citations
Samplen = 12 Pat.
Durationsingle test dose with 240…
EndpointNRS
Blindingoffen
DesignKlinische Studie
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding
Significant reduction in spasticity (NRS scores from median 6 to 3.5, p<0.001) with inverse correlation to THC/CBD plasma concentrations; no significant effects in motor tests.
Summary
Pilot study n=12 MS patients with THC/CBD spray (2 sprays); peak plasma concentrations THC 0,60–13,29 ng/mL, CBD 0,55–11,93 ng/mL. NRS spasticity score decreased median from 6 to 3,5 (p<0,001); significant inverse correlation between NRS and THC plasma concentration (p<0,01) as well as CBD plasma concentration (p<0,002).
P
PopulationAdults with multiple sclerosis (chronically treated), n=12
I
InterventionTHC/CBD oromucosal spray, 2 sprays at 15-minute intervals (test dose), subacute single dose
O
OutcomeNRS spasticity score decreased from median 6 to 3,5 (p<0,001); significant inverse correlation between NRS and THC plasma concentration (p<0,01) as well as CBD plasma concentration (p<0,002); no significant effects in posturographic and motor tests
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
Open-label
Effect size
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Objectives: We aimed to assess the potential relationship between intrasubject 9-tetrahydrocannabinol/cannabidiol (THC/CBD) oromucosal spray plasma profiles and clinical effects elicited by subacute dosing in chronically treated patients with multiple sclerosis (MS).
Methods: The study design was pilot, single center, open, and prospective. The patients were challenged with a morning test dose of 2 THC/CBD sprays at a 15-minute interval. Venous blood samples were collected before the first spray administration and every 30 minutes after the second spray, until 240 minutes postdosing. Patients rated their spasticity by the Numerical Rating Scale (NRS) simultaneously with blood drawings. Postural and motor tests were performed before the first spray and 90 and 180 minutes thereafter.
Results: Twelve patients were recruited. Peak plasma concentrations of THC/CBD largely varied among patients, from 0.60 to 13.29 ng/mL for THC and 0.55 to 11.93 ng/mL for CBD. Time to peak plasma concentrations ranged from 150 to 240 minutes for THC and 90 to 240 minutes for CBD. Patients' NRS serial scores decreased after dosing, from a median value of 6 to 3.5 (P < 0.001). A significant inverse correlation was observed between median intrasubject repeated NRS scores and corresponding median values of both THC (P < 0.01) and CBD (P < 0.002) plasma concentrations. No significant effect of cannabinoids dosing could be appreciated according to posturographic and motor tests.
Conclusions: Our kinetic dynamic findings from THC/CBD oromucosal spray are the first obtained in real MS patients. Although preliminary, they suggest that subacute dosing might elicit a subjective clinically significant effect on MS-related spasticity, paralleling cannabinoids measurable plasma concentrations.
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