The effect of mianserin add-on, on the intensity of opioid withdrawal symptoms during detoxification program-a randomized, double blind, placebo ... study [An article from: Addictive Behaviors] Buy on Amazon
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The effect of mianserin add-on, on the intensity of opioid withdrawal symptoms during detoxification program-a randomized, double blind, placebo ... study [An article from: Addictive Behaviors]

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Book Details
Publisher Elsevier
ISBN / ASIN B000RR4AWA
ISBN-13 978B000RR4AW0
Availability Available for download now
Sales Rank #99,999,999
Marketplace United States 🇺🇸
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This digital document is a journal article from Addictive Behaviors, published by Elsevier in 2005. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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Background: Based on pre-clinical studies regarding the interaction of various antidepressant drugs with the opioid system, we designed a clinical study to be carried out in the 'in-patient detoxification unit' within a large community centre for treatment of drugs dependent people. We evaluated the effect of mianserin add-on, on the intensity of opioid withdrawal symptoms in opiate dependent subjects undergoing medication-supported physical detoxification and integrated psychosocial and psychotherapeutic intervention for the treatment of dependence. Methods: Mianserin (or placebo) was added to the routine medication protocol, during the 3-week in-patient phase of detoxification in a prospective, randomized, double blind, placebo controlled study. Mianserin (or placebo) was continued after discharge and patients were followed up for 3 months in order to evaluate relapse rates. Opiate withdrawal symptoms were assessed during the first 10 days, while depression and anxiety were assessed throughout the 3 months of study. Results: From day 2 onward, patients in the study group showed significantly lower withdrawal symptoms than the control group patients and reached this peak faster (study group 2.8 days, control group 3.2 days, p
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