Abstract | OBJECTIVE: DESIGN: Parallel-group, randomized, placebo-controlled trial. BACKGROUND SETTING:
Coenzyme Q(10) has been shown to boost muscle energy metabolism in post- polio subjects but it does not promote muscle strength, endurance or function in polio survivors with post-poliomyelitis syndrome. However, the collective increased energy metabolism might contribute to a reduction in post- polio fatigue. PARTICIPANTS: METHOD: Participants were assigned (1:1), with stratification of those who use energy-saving mobility aids, to receive 100 mg coenzyme Q(10) or matching placebo daily for 60 days. Participants and investigators were blinded to group allocation. Fatigue was assessed by the Multidimensional Assessment of Fatigue as the primary outcome and the Fatigue Severity Scale as secondary outcome. RESULTS: Of 103 participants, 54 were assigned to receive coenzyme Q(10) and 49 to receive the placebo. The difference in the mean score reductions between the two groups was not statistically significant for either fatigue measure. Oral supplementation with coenzyme Q(10) was safe and well-tolerated. CONCLUSION: A daily dose of 100 mg coenzyme Q(10) for 60 days does not alleviate the fatigue of the late-onset sequelae of poliomyelitis. The registration number for the clinical trial is ACTRN 12612000552886.
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Authors | Margaret M Peel, Marie Cooke, Helen J Lewis-Peel, Rodney A Lea, Wendy Moyle |
Journal | Complementary therapies in medicine
(Complement Ther Med)
Vol. 23
Issue 6
Pg. 789-93
(Dec 2015)
ISSN: 1873-6963 [Electronic] Scotland |
PMID | 26645517
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Aged
- Australia
- Fatigue
(drug therapy, etiology)
- Female
- Humans
- Male
- Middle Aged
- Poliomyelitis
(complications)
- Ubiquinone
(administration & dosage, adverse effects, analogs & derivatives, therapeutic use)
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