Low-dose naltrexone for the treatment of fibromyalgia: findings of a small,
randomized, double-blind, placebo-controlled, counterbalanced, crossover trial
assessing daily pain levels.
Author(s): Younger J(1), Noor N, McCue R, Mackey S.
Affiliation(s): Author information:
(1)Stanford University School of Medicine, Palo Alto, California 94304-1573, USA.
jarred.younger@stanford.edu
Publication date & source: 2013, Arthritis Rheum. , 65(2):529-38
OBJECTIVE: To determine whether low dosages (4.5 mg/day) of naltrexone reduce
fibromyalgia severity as compared with the nonspecific effects of placebo. In
this replication and extension study of a previous clinical trial, we tested the
impact of low-dose naltrexone on daily self-reported pain. Secondary outcomes
included general satisfaction with life, positive mood, sleep quality, and
fatigue.
METHODS: Thirty-one women with fibromyalgia participated in the randomized,
double-blind, placebo-controlled, counterbalanced, crossover study. During the
active drug phase, participants received 4.5 mg of oral naltrexone daily. An
intensive longitudinal design was used to measure daily levels of pain.
RESULTS: When contrasting the condition end points, we observed a significantly
greater reduction of baseline pain in those taking low-dose naltrexone than in
those taking placebo (28.8% reduction versus 18.0% reduction; P = 0.016).
Low-dose naltrexone was also associated with improved general satisfaction with
life (P = 0.045) and with improved mood (P = 0.039), but not improved fatigue or
sleep. Thirty-two percent of participants met the criteria for response (defined
as a significant reduction in pain plus a significant reduction in either fatigue
or sleep problems) during low-dose naltrexone therapy, as contrasted with an 11%
response rate during placebo therapy (P = 0.05). Low-dose naltrexone was rated
equally tolerable as placebo, and no serious side effects were reported.
CONCLUSION: The preliminary evidence continues to show that low-dose naltrexone
has a specific and clinically beneficial impact on fibromyalgia pain. The
medication is widely available, inexpensive, safe, and well-tolerated.
Parallel-group randomized controlled trials are needed to fully determine the
efficacy of the medication.
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