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Methadone induction in primary care (ANRS-Methaville): a phase III randomized intervention trial
In France, the rapid scale-up of buprenorphine, an opioid maintenance treatment (OMT), in primary care for drug users has led to an impressive reduction in HIV prevalence among injecting drug users (IDU) but has had no major effect on Hepatitis C incidence. To date, patients willing to start methado...
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Published in: | BMC public health 2012-06, Vol.12 (1), p.488-488, Article 488 |
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description | In France, the rapid scale-up of buprenorphine, an opioid maintenance treatment (OMT), in primary care for drug users has led to an impressive reduction in HIV prevalence among injecting drug users (IDU) but has had no major effect on Hepatitis C incidence. To date, patients willing to start methadone can only do so in a methadone clinic (a medical centre for drug and alcohol dependence (CSAPA) or a hospital setting) and are referred to primary care physicians after dose stabilization. This study aims to assess the effectiveness of methadone in patients who initiated treatment in primary care compared with those who initiated it in a CSAPA, by measuring abstinence from street opioid use after one year of treatment.
The ANRS-Methaville study is a randomized multicenter non-inferiority control trial comparing methadone induction (lasting approximately 2 weeks) in primary care and in CSAPA. The model of care chosen for methadone induction in primary care was based on study-specific pre-training of all physicians, exclusion criteria and daily supervision of methadone during the initiation phase. Between January 2009 and January 2011, 10 sites each having one CSAPA and several primary care physicians, were identified to recruit patients to be randomized into two groups, one starting methadone in primary care (n = 147), the other in CSAPA (n = 48). The primary outcome of the study is the proportion of participants abstinent from street opioids after 1 year of treatment i.e. non-inferiority of primary care model in terms of the proportion of patients not using street opioids compared with the proportion observed in those starting methadone in a CSAPA.
The ANRS-Methaville study is the first in France to use an interventional trial to improve access to OMT for drug users. Once the non-inferiority results become available, the Ministry of Health and agency for the safety of health products may change the the New Drug Application (NDA) of methadone and make methadone induction by trained primary care physicians possible.The trial is registered with the French Agency of Pharmaceutical Products (AFSSAPS) under the number 2008-A0277-48, the European Union Drug Regulating Authorities Clinical Trials.Number Eudract 2008-001338-28, the ClinicalTrials.gov Identifier: NCT00657397 and the International Standard Randomised Controlled Trial Number Register ISRCTN31125511. |
doi_str_mv | 10.1186/1471-2458-12-488 |
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The ANRS-Methaville study is a randomized multicenter non-inferiority control trial comparing methadone induction (lasting approximately 2 weeks) in primary care and in CSAPA. The model of care chosen for methadone induction in primary care was based on study-specific pre-training of all physicians, exclusion criteria and daily supervision of methadone during the initiation phase. Between January 2009 and January 2011, 10 sites each having one CSAPA and several primary care physicians, were identified to recruit patients to be randomized into two groups, one starting methadone in primary care (n = 147), the other in CSAPA (n = 48). The primary outcome of the study is the proportion of participants abstinent from street opioids after 1 year of treatment i.e. non-inferiority of primary care model in terms of the proportion of patients not using street opioids compared with the proportion observed in those starting methadone in a CSAPA.
The ANRS-Methaville study is the first in France to use an interventional trial to improve access to OMT for drug users. Once the non-inferiority results become available, the Ministry of Health and agency for the safety of health products may change the the New Drug Application (NDA) of methadone and make methadone induction by trained primary care physicians possible.The trial is registered with the French Agency of Pharmaceutical Products (AFSSAPS) under the number 2008-A0277-48, the European Union Drug Regulating Authorities Clinical Trials.Number Eudract 2008-001338-28, the ClinicalTrials.gov Identifier: NCT00657397 and the International Standard Randomised Controlled Trial Number Register ISRCTN31125511.</description><identifier>ISSN: 1471-2458</identifier><identifier>EISSN: 1471-2458</identifier><identifier>DOI: 10.1186/1471-2458-12-488</identifier><identifier>PMID: 22741944</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Alcohol ; Alcoholism ; Benzodiazepines ; Buprenorphine ; Care and treatment ; Central nervous system depressants ; Clinical trials ; Comparative analysis ; Design ; Drug dosages ; Drug interactions ; Drug overdose ; Drug therapy ; Follow-Up Studies ; France ; Health aspects ; Hepatitis C ; Humans ; Initiation ; Life Sciences ; Medical centers ; Medical research ; Medicine, Experimental ; Methadone ; Methadone - therapeutic use ; Methadone hydrochloride ; Narcotics ; Opiate Substitution Treatment - methods ; Opioid maintenance treatment ; Opioid use ; Opioid-Related Disorders - drug therapy ; Overdose ; Patients ; Physicians ; Primary care ; Primary Health Care - organization & administration ; Product development ; Santé publique et épidémiologie ; Study Protocol ; Substance Abuse Treatment Centers ; Time Factors ; Treatment Outcome</subject><ispartof>BMC public health, 2012-06, Vol.12 (1), p.488-488, Article 488</ispartof><rights>COPYRIGHT 2012 BioMed Central Ltd.</rights><rights>2012 Roux et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright ©2012 Roux et al.; licensee BioMed Central Ltd. 2012 Roux et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b654t-62c8061713dc8b0fb9ad1e7e6bc280d9c224f7532bc18ad3577143642a26df853</citedby><cites>FETCH-LOGICAL-b654t-62c8061713dc8b0fb9ad1e7e6bc280d9c224f7532bc18ad3577143642a26df853</cites><orcidid>0000-0002-3546-8020 ; 0000-0002-5069-4982 ; 0000-0002-6794-4837</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528472/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1242075890?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22741944$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-00768513$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Roux, Perrine</creatorcontrib><creatorcontrib>Michel, Laurent</creatorcontrib><creatorcontrib>Cohen, Julien</creatorcontrib><creatorcontrib>Mora, Marion</creatorcontrib><creatorcontrib>Morel, Alain</creatorcontrib><creatorcontrib>Aubertin, Jean-Francois</creatorcontrib><creatorcontrib>Desenclos, Jean-Claude</creatorcontrib><creatorcontrib>Spire, Bruno</creatorcontrib><creatorcontrib>Carrieri, Patrizia M</creatorcontrib><creatorcontrib>ANRS Methaville Study Group</creatorcontrib><creatorcontrib>and the ANRS Methaville Study Group</creatorcontrib><title>Methadone induction in primary care (ANRS-Methaville): a phase III randomized intervention trial</title><title>BMC public health</title><addtitle>BMC Public Health</addtitle><description>In France, the rapid scale-up of buprenorphine, an opioid maintenance treatment (OMT), in primary care for drug users has led to an impressive reduction in HIV prevalence among injecting drug users (IDU) but has had no major effect on Hepatitis C incidence. To date, patients willing to start methadone can only do so in a methadone clinic (a medical centre for drug and alcohol dependence (CSAPA) or a hospital setting) and are referred to primary care physicians after dose stabilization. This study aims to assess the effectiveness of methadone in patients who initiated treatment in primary care compared with those who initiated it in a CSAPA, by measuring abstinence from street opioid use after one year of treatment.
The ANRS-Methaville study is a randomized multicenter non-inferiority control trial comparing methadone induction (lasting approximately 2 weeks) in primary care and in CSAPA. The model of care chosen for methadone induction in primary care was based on study-specific pre-training of all physicians, exclusion criteria and daily supervision of methadone during the initiation phase. Between January 2009 and January 2011, 10 sites each having one CSAPA and several primary care physicians, were identified to recruit patients to be randomized into two groups, one starting methadone in primary care (n = 147), the other in CSAPA (n = 48). The primary outcome of the study is the proportion of participants abstinent from street opioids after 1 year of treatment i.e. non-inferiority of primary care model in terms of the proportion of patients not using street opioids compared with the proportion observed in those starting methadone in a CSAPA.
The ANRS-Methaville study is the first in France to use an interventional trial to improve access to OMT for drug users. Once the non-inferiority results become available, the Ministry of Health and agency for the safety of health products may change the the New Drug Application (NDA) of methadone and make methadone induction by trained primary care physicians possible.The trial is registered with the French Agency of Pharmaceutical Products (AFSSAPS) under the number 2008-A0277-48, the European Union Drug Regulating Authorities Clinical Trials.Number Eudract 2008-001338-28, the ClinicalTrials.gov Identifier: NCT00657397 and the International Standard Randomised Controlled Trial Number Register ISRCTN31125511.</description><subject>Alcohol</subject><subject>Alcoholism</subject><subject>Benzodiazepines</subject><subject>Buprenorphine</subject><subject>Care and treatment</subject><subject>Central nervous system depressants</subject><subject>Clinical trials</subject><subject>Comparative analysis</subject><subject>Design</subject><subject>Drug dosages</subject><subject>Drug interactions</subject><subject>Drug overdose</subject><subject>Drug therapy</subject><subject>Follow-Up Studies</subject><subject>France</subject><subject>Health aspects</subject><subject>Hepatitis C</subject><subject>Humans</subject><subject>Initiation</subject><subject>Life Sciences</subject><subject>Medical centers</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Methadone</subject><subject>Methadone - therapeutic use</subject><subject>Methadone hydrochloride</subject><subject>Narcotics</subject><subject>Opiate Substitution Treatment - methods</subject><subject>Opioid maintenance treatment</subject><subject>Opioid use</subject><subject>Opioid-Related Disorders - drug therapy</subject><subject>Overdose</subject><subject>Patients</subject><subject>Physicians</subject><subject>Primary care</subject><subject>Primary Health Care - organization & administration</subject><subject>Product development</subject><subject>Santé publique et épidémiologie</subject><subject>Study Protocol</subject><subject>Substance Abuse Treatment Centers</subject><subject>Time Factors</subject><subject>Treatment 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induction in primary care (ANRS-Methaville): a phase III randomized intervention trial</title><author>Roux, Perrine ; Michel, Laurent ; Cohen, Julien ; Mora, Marion ; Morel, Alain ; Aubertin, Jean-Francois ; Desenclos, Jean-Claude ; Spire, Bruno ; Carrieri, Patrizia M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b654t-62c8061713dc8b0fb9ad1e7e6bc280d9c224f7532bc18ad3577143642a26df853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Alcohol</topic><topic>Alcoholism</topic><topic>Benzodiazepines</topic><topic>Buprenorphine</topic><topic>Care and treatment</topic><topic>Central nervous system depressants</topic><topic>Clinical trials</topic><topic>Comparative analysis</topic><topic>Design</topic><topic>Drug dosages</topic><topic>Drug interactions</topic><topic>Drug overdose</topic><topic>Drug therapy</topic><topic>Follow-Up Studies</topic><topic>France</topic><topic>Health 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intervention trial</atitle><jtitle>BMC public health</jtitle><addtitle>BMC Public Health</addtitle><date>2012-06-28</date><risdate>2012</risdate><volume>12</volume><issue>1</issue><spage>488</spage><epage>488</epage><pages>488-488</pages><artnum>488</artnum><issn>1471-2458</issn><eissn>1471-2458</eissn><abstract>In France, the rapid scale-up of buprenorphine, an opioid maintenance treatment (OMT), in primary care for drug users has led to an impressive reduction in HIV prevalence among injecting drug users (IDU) but has had no major effect on Hepatitis C incidence. To date, patients willing to start methadone can only do so in a methadone clinic (a medical centre for drug and alcohol dependence (CSAPA) or a hospital setting) and are referred to primary care physicians after dose stabilization. This study aims to assess the effectiveness of methadone in patients who initiated treatment in primary care compared with those who initiated it in a CSAPA, by measuring abstinence from street opioid use after one year of treatment.
The ANRS-Methaville study is a randomized multicenter non-inferiority control trial comparing methadone induction (lasting approximately 2 weeks) in primary care and in CSAPA. The model of care chosen for methadone induction in primary care was based on study-specific pre-training of all physicians, exclusion criteria and daily supervision of methadone during the initiation phase. Between January 2009 and January 2011, 10 sites each having one CSAPA and several primary care physicians, were identified to recruit patients to be randomized into two groups, one starting methadone in primary care (n = 147), the other in CSAPA (n = 48). The primary outcome of the study is the proportion of participants abstinent from street opioids after 1 year of treatment i.e. non-inferiority of primary care model in terms of the proportion of patients not using street opioids compared with the proportion observed in those starting methadone in a CSAPA.
The ANRS-Methaville study is the first in France to use an interventional trial to improve access to OMT for drug users. Once the non-inferiority results become available, the Ministry of Health and agency for the safety of health products may change the the New Drug Application (NDA) of methadone and make methadone induction by trained primary care physicians possible.The trial is registered with the French Agency of Pharmaceutical Products (AFSSAPS) under the number 2008-A0277-48, the European Union Drug Regulating Authorities Clinical Trials.Number Eudract 2008-001338-28, the ClinicalTrials.gov Identifier: NCT00657397 and the International Standard Randomised Controlled Trial Number Register ISRCTN31125511.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>22741944</pmid><doi>10.1186/1471-2458-12-488</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3546-8020</orcidid><orcidid>https://orcid.org/0000-0002-5069-4982</orcidid><orcidid>https://orcid.org/0000-0002-6794-4837</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_doaj_primary_oai_doaj_org_article_b03a066441bc40399575a5ff6fc23a69 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central |
subjects | Alcohol Alcoholism Benzodiazepines Buprenorphine Care and treatment Central nervous system depressants Clinical trials Comparative analysis Design Drug dosages Drug interactions Drug overdose Drug therapy Follow-Up Studies France Health aspects Hepatitis C Humans Initiation Life Sciences Medical centers Medical research Medicine, Experimental Methadone Methadone - therapeutic use Methadone hydrochloride Narcotics Opiate Substitution Treatment - methods Opioid maintenance treatment Opioid use Opioid-Related Disorders - drug therapy Overdose Patients Physicians Primary care Primary Health Care - organization & administration Product development Santé publique et épidémiologie Study Protocol Substance Abuse Treatment Centers Time Factors Treatment Outcome |
title | Methadone induction in primary care (ANRS-Methaville): a phase III randomized intervention trial |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T17%3A50%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Methadone%20induction%20in%20primary%20care%20(ANRS-Methaville):%20a%20phase%20III%20randomized%20intervention%20trial&rft.jtitle=BMC%20public%20health&rft.au=Roux,%20Perrine&rft.aucorp=ANRS%20Methaville%20Study%20Group&rft.date=2012-06-28&rft.volume=12&rft.issue=1&rft.spage=488&rft.epage=488&rft.pages=488-488&rft.artnum=488&rft.issn=1471-2458&rft.eissn=1471-2458&rft_id=info:doi/10.1186/1471-2458-12-488&rft_dat=%3Cgale_doaj_%3EA534158945%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b654t-62c8061713dc8b0fb9ad1e7e6bc280d9c224f7532bc18ad3577143642a26df853%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1242075890&rft_id=info:pmid/22741944&rft_galeid=A534158945&rfr_iscdi=true |