Abstract | OBJECTIVE: METHODS: In a double blind placebo-controlled clinical trial, the efficacy of 8 mg/day of reboxetine (twice daily) was compared with placebo in 40 adults diagnosed with ADHD during 6 weeks. The measures were Conners' Adult ADHD Rating Scale-Self-Report, Screening Version (CAARS-S, SV), Hamilton Anxiety and Depression Rating Scales, Clinical Global Impression - Severity Scale (CGI-S), and Global Assessment of Functioning Scale (GAF). RESULTS: There was a main effect of time and significant time X treatment ( reboxetine vs. placebo) interaction on CAARS subscales and CGI scores which decreased along the study (p < 0.01). There was also a main effect of time and time X treatment interaction on GAF score which increased at the end point of the study (p < 0.01). In terms of Hamilton Anxiety and Depression Rating Scales there was just a main effect of time on Hamilton Depression Scale (p < 0.01). Irritability, anxiety, sleep disturbance, and dry mouth were the common side effects of reboxetine. CONCLUSION:
Reboxetine could be used and tolerated as an effective treatment for adults with ADHD.
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Authors | Forough Riahi, Mehdi Tehrani-Doost, Zahra Shahrivar, Javad Alaghband-Rad |
Journal | Human psychopharmacology
(Hum Psychopharmacol)
Vol. 25
Issue 7-8
Pg. 570-6
(Nov 2010)
ISSN: 1099-1077 [Electronic] England |
PMID | 21312292
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 John Wiley & Sons, Ltd. |
Chemical References |
- Antidepressive Agents
- Morpholines
- Placebos
- Reboxetine
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Topics |
- Adult
- Antidepressive Agents
(adverse effects, therapeutic use)
- Attention Deficit Disorder with Hyperactivity
(drug therapy)
- Double-Blind Method
- Female
- Humans
- Male
- Morpholines
(adverse effects, therapeutic use)
- Placebos
- Psychiatric Status Rating Scales
- Reboxetine
- Treatment Outcome
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