Studienlage · Detail
Klarer Nutzen
GRADE
Moderat
101 Zitate
Stichproben = 26 Pat.
Dauer8 Wochen pro Behandlungsphase…
KontrolleIbuprofen 400 mg/Tag oral, 8 Wochen
EndpunktSchmerzintensität
Verblindungdoppelblind
DesignRCT (doppelblind, aktiv-kontrolliert, Crossover)
Cannabinoidthc
Max. Dosis0.5 mg
Applikationoral
Kernaussage
Nabilone reduzierte Schmerzintensität, Analgetikakonsum und Medikamentenabhängigkeit signifikant stärker als Ibuprofen.
Zusammenfassung
n=26 Patienten mit chronisch intraktablem Medication-Overuse-Headache (MOH), Nabilone 0,5 mg/Tag vs. Ibuprofen 400 mg/Tag, 8 Wochen Crossover; Nabilone signifikant überlegen bei Schmerzintensität (p<0,05) und täglichem Analgetikakonsum (p<0,05). Nur Nabilone reduzierte Medikamenten-Abhängigkeitsgrad (−41%, p<0,01) und verbesserte Lebensqualität (p<0,05). Erster RCT zu Cannabinoiden bei MOH.
P
PopulationErwachsene mit therapierefraktärem Medikamentenübergebrauchskopfschmerz (MOH), n=30 (26 Completers)
I
InterventionNabilone 0,5 mg/Tag oral, 8 Wochen
C
KontrolleIbuprofen 400 mg/Tag oral, 8 Wochen
O
OutcomeNabilone signifikant wirksamer als Ibuprofen bei Schmerzintensität und täglicher Analgetikaeinnahme (p<0,05); Reduktion der Medikamentenabhängigkeit –41% (p<0,01); Verbesserung der Lebensqualität (p<0,05)
Vertrauen in die Evidenz
Moderat
Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.
Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Klarer Nutzen
Zitate / Jahr
★★★★★
Autoren
Teilen
Abstract
Medication overuse headache (MOH) is a severe burden to sufferers and its treatment has few evidence-based indications. The aim of this study is to evaluate efficacy and safety of nabilone in reducing pain and frequency of headache, the number of analgesic intake and in increasing the quality of life on patients with long-standing intractable MOH. Thirty MOH patients were enrolled at the University of Modena's Interdepartmental Centre for Research on Headache and Drug Abuse (Italy) in a randomized, double-blind, active-controlled, crossover study comparing nabilone 0.5 mg/day and ibuprofen 400 mg. The patients received each treatment orally for 8 weeks (before nabilone and then ibuprofen or vice versa), with 1 week wash-out between them. Randomization and allocation (ratio 1:1) were carried out by an independent pharmacy through a central computer system. Participants, care givers, and those assessing the outcomes were blinded to treatment sequence. Twenty-six subjects completed the study. Improvements from baseline were observed with both treatments. However, nabilone was more effective than ibuprofen in reducing pain intensity and daily analgesic intake (p < 0.05); moreover, nabilone was the only drug able to reduce the level of medication dependence (-41 %, p < 0.01) and to improve the quality of life (p < 0.05). Side effects were uncommon, mild and disappeared when nabilone was discontinued. This is the first randomized controlled trial demonstrating the benefits of nabilone on headache, analgesic consumption and the quality of life in patients with intractable MOH. This drug also appears to be safe and well-tolerated. Larger scale studies are needed to confirm these preliminary findings.
„Was dem Handeln im Weg steht, wird zum Weg.“