Study register · detail
Clear benefit
GRADE
Low
57 citations
Samplen = 124 Pat.
Durationaverage 7 months
EndpointNRS
Blindingn.a.
DesignMultizentrische retrospektive Umfrage
Cannabinoidthc
Max. dose7.5 mg
Routeoral
Key finding
Delta-9-THC significantly reduced pain intensity and improved psychometric parameters, with an acceptable side effect profile in the majority of patients.
Summary
Multicentre retrospective telephone survey: n=172 patients with central neuropathic pain and fibromyalgia received on average 7,5 mg Delta-9-THC over 7 months; n=124 evaluable (48 premature discontinuation). Psychometric parameters (PDI, SF-12, QLIP, HADS) as well as pain intensity (NRS) improved significantly; opioid doses were reduced. ~25% of patients did not tolerate the treatment.
P
PopulationAdults with chronic central neuropathic pain syndrome and fibromyalgia, n=124 (evaluated), originally n=172
I
InterventionDelta-9-THC oral, average 7,5 mg/day over approximately 7 months
O
OutcomeSignificant improvement in pain intensity (NRS), PDI, SF-12, QLIP and HADS; reduction of opioid doses; approximately 25% treatment discontinuation due to side effects
Confidence in the evidence
Low
The second of four GRADE levels, the effect estimate is of limited reliability.
Quality profile
Sample size
★★★★★
Blinding
—
Effect size
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Central neuropathic pain is difficult to treat, but delta 9-Tetrahydrocannabinol (delta 9-THC) may be a promising therapeutic agent. We administered in 172 patients on average 7.5 mg delta 9-THC over 7 months. Of these, 48 patients prematurely withdrew due to side effects, insufficient analgesia, or expense of therapy. Thus, 124 patients were assessed retrospectively in a multicenter telephone survey. Reported changes in pain intensity, recorded on a numeric rating scale (NRS), Pain Disability Index (PDI), Medical Outcomes Short-Form (SF-12), Quality of Life Impairment by Pain (QLIP), Hospital Anxiety Depression Scale (HADS), and amount of concomitant pain medication were recorded. Psychometric parameters (PDI, SF-12, QLIP, HADS) and pain intensity improved significantly during delta 9-THC treatment. Opioid doses were reduced and patients perceived THC therapy as effective with tolerable side effects. About 25% of the patients, however, did not tolerate the treatment. Therapy success and tolerance can be assessed by a transient delta 9-THC titration and its maintained administration for several weeks. The present survey demonstrates its ameliorating potential for the treatment of chronic pain in central neuropathy and fibromyalgia. A supplemental delta 9-THC treatment as part of a broader pain management plan therefore may represent a promising coanalgesic therapeutic option.
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