Abstract |
119 patients were enrolled in a double-blind randomized parallel study versus placebo carried out to assess both the efficacy and tolerability of L-deprenyl (10 mg/day) for treatment of patients with organic mental disorders of the Alzheimer type (DAT). The treatments were given for 3 months, starting after a run-in period of 15 days to evaluate efficacy. A complete neuropsychological battery was administered monthly after the start of treatment whereas tolerability was assessed by checking, recording and classifying all the unfavorable experiences occurring. According to the results, L-deprenyl would seem to be a useful and reliable tool for the treatment of DAT patients in an attempt to improve their cognitive functions and reduce behavioral alterations, without frequent or severe side effects.
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Authors | A Mangoni, M P Grassi, L Frattola, R Piolti, S Bassi, A Motta, A Marcone, S Smirne |
Journal | European neurology
(Eur Neurol)
Vol. 31
Issue 2
Pg. 100-7
( 1991)
ISSN: 0014-3022 [Print] Switzerland |
PMID | 1904354
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
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Topics |
- Activities of Daily Living
- Aged
- Alzheimer Disease
(drug therapy)
- Double-Blind Method
- Humans
- Male
- Middle Aged
- Neuropsychological Tests
- Prognosis
- Selegiline
(adverse effects, therapeutic use)
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