Modafinil for fatigue in MS
A randomized placebo-controlled double-blind study
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Abstract
Objective: To assess whether modafinil, a wakefulness-promoting agent, is useful for fatigue in patients with multiple sclerosis (MS).
Methods: Patients with MS with stable disability, and a baseline score of 45 or more on the Modified Fatigue Impact Scale (MFIS), were eligible for the 5-week randomized, double-blind, placebo-controlled, parallel group study. The initial daily dose of modafinil was 200 mg for 1 week. Depending on tolerance, the dose was increased by 100 mg every week up to 400 mg/day and remained unchanged between day 21 and day 35. The primary outcome variable was the change of MFIS score at day 35.
Results: A total of 115 patients with MS were enrolled in the study and in the intention to treat analysis. The mean MFIS score at baseline was 63 ± 9 in the placebo group and 63 ± 10 in the modafinil group. MFIS scores improved between day 0 and day 35 in both placebo-treated and modafinil-treated groups, but no significant difference was detected between the two groups. There was no major safety concern.
Conclusions: There was no improvement of fatigue in patients with multiple sclerosis treated with modafinil vs placebo according to the Modified Fatigue Impact Scale.
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Disputes & Debates: Rapid online correspondence
- Reply to Kraft et al
- Bruno Stankoff, Centre d'Investigation Clinique, Hôpital de la Salpetrière, 47 Bd de l'Hopital, 75651 Paris Cedex 13bruno.stankoff@psl.ap-hop-paris.fr
- Emmanuelle Waubant, Catherine Lubetzki, Michel Clanet for the French Modafinil Study Group
Submitted June 13, 2005 - Modafinil for fatigue in MS: A randomized placebo-controlled double-blind study
- George H. Kraft, University of Washington, 1959 NE Pacific St, Box 356490, Seattle, WA 98195msrrtc@u.washington.edu
- James Bowen
Submitted June 13, 2005 - Modafinil for fatigue in MS: A randomized placebo-controlled double-blind study
- Kottil W. Rammohan, Ohio State University, 2050 Kenney Road, OSU MS Center, Martha Morehouse Medical Plaza, Columbus, Ohio 43221rammohan.2@osu.edu
- Deborah Joanne Lynn
Submitted June 07, 2005 - Reply to Rammohan et al
- Bruno Stankoff, Centre d'Investigation Clinique, Hôpital de la Salpêtrière, 47 Bd de L'Hôpital, 75651, Paris cedex 13, Francebruno.stankoff@psl.ap-hop-paris.fr
- Emmanuelle Waubant, Catherine Lubetzki, Michel Clanet for the French Modafinil Study Group
Submitted June 07, 2005
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