Studienlage · Detail
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GRADE
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68 Zitate
Stichproben = 25 Pat.
Dauerdrei Phasen à 6 Wochen
KontrollePlacebo
EndpunktSpastik-Summen-Score
Verblindungdoppelblind
DesignOpen-Label-Studie + kleine RCT-Phase
Cannabinoidthc
Max. Dosis43.0 mg
Applikationoral
Kernaussage
THC reduzierte den Spastik-Summen-Score gegenüber Baseline und Placebo signifikant (p=0,001).
Zusammenfassung
n=25 Patienten mit Rückenmarksverletzung; orales THC (mittlere Tagesdosis 31 mg) senkte den Spastizitäts-Summen-Score (SSS, Modified Ashworth Scale) signifikant von 16,72 auf 8,92 (p=0,001); THC-HS rektal zeigte ähnliche Wirkung.
P
PopulationErwachsene mit Rückenmarksverletzung (SCI), n=25
I
InterventionOrales THC (Startdosis 10 mg, mittlere Tagesdosis 31 mg) und rektales THC-Hemisuccinat (THC-HS, mittlere Tagesdosis 43 mg), 6-wöchige Phasen
C
KontrollePlacebo (orale Kapsel, Phase 3, n=7)
O
OutcomeSSS (MAS) sank unter THC signifikant von 16,72 auf 8,92 (Tag 43); signifikante Verbesserung des SSS unter Verumbehandlung vs. Placebo (p=0,001)
Vertrauen in die Evidenz
Niedrig
Zweite von vier GRADE-Stufen, die Effektschätzung ist begrenzt verlässlich.
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VerzerrungsrisikoUngenauigkeit
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Klarer Nutzen
Zitate / Jahr
★★★★★
Autoren
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Abstract
<h4>Study design</h4>Open label study to determine drug dose for a randomized double-blind placebo-controlled parallel study.<h4>Objectives</h4>To assess the efficacy and side effects of oral Delta(9)-tetrahydrocannabinol (THC) and rectal THC-hemisuccinate (THC-HS) in SCI patients.<h4>Setting</h4>REHAB Basel, Switzerland.<h4>Method</h4>Twenty-five patients with SCI were included in this three-phase study with individual dose adjustment, each consisting of 6 weeks. Twenty-two participants received oral THC open label starting with a single dose of 10 mg (Phase 1, completed by 15 patients). Eight subjects received rectal THC-HS (Phase 2, completed by seven patients). In Phase 3, six patients were treated with oral THC and seven with placebo. Major outcome parameters were the spasticity sum score (SSS) using the Modified Ashworth Scale (MAS) and self-ratings of spasticity.<h4>Results</h4>Mean daily doses were 31 mg with THC and 43 mg with THC-HS. Mean SSS for THC decreased significantly from 16.72 (+/-7.60) at baseline to 8.92 (+/-7.14) on day 43. Similar improvement was seen with THC-HS. We observed a significant improvement of SSS with active drug (P=0.001) in the seven subjects who received oral THC in Phase 1 and placebo in Phase 3. Major reasons for drop out were increase of pain and psychological side effects.<h4>Conclusion</h4>THC is an effective and safe drug in the treatment of spasticity. At least 15-20 mg per day were needed to achieve a therapeutic effect.
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