Abstract |
Chronic normal-dose benzodiazepine users requesting drug withdrawal were allocated to substitution with either the new anxiolytic alpidem (n = 13) or placebo (n = 12). During the first 2 weeks of the tapering programme, the dose of benzodiazepine was kept constant; for the next 2 weeks it was halved and half-dose alpidem (25 mg twice daily) or placebo substituted; for weeks 5 and 6, the benzodiazepine was discontinued and full-dose alpidem or placebo given; next alpidem or placebo were tapered to half-dose and then finally discontinued. Regular anxiety and tranquillizer withdrawal ratings were made. Nine of 12 patients given placebo withdrew successfully compared with four of 13 alpidem-treated patients. Anxiety and other symptom levels increased in the alpidem but not the placebo patients. It was concluded that alpidem is not helpful in helping patients withdrawing from a benzodiazepine withdrawal perhaps because of partial agonist properties. These actions may imply a lesser propensity to induce dependence on long-term use.
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Authors | M Lader, I Farr, S Morton |
Journal | International clinical psychopharmacology
(Int Clin Psychopharmacol)
Vol. 8
Issue 1
Pg. 31-6
( 1993)
ISSN: 0268-1315 [Print] England |
PMID | 8097214
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Anti-Anxiety Agents
- Imidazoles
- Pyridines
- Benzodiazepines
- alpidem
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Topics |
- Adult
- Anti-Anxiety Agents
(adverse effects, therapeutic use)
- Anxiety
(drug therapy)
- Benzodiazepines
- Female
- Humans
- Imidazoles
(therapeutic use)
- Male
- Middle Aged
- Prognosis
- Psychiatric Status Rating Scales
- Pyridines
(therapeutic use)
- Regression Analysis
- Substance Withdrawal Syndrome
(drug therapy, psychology)
- Time Factors
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