OPAL: "Opiates and PhArmacoLogy"

Sponsor
Nantes University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01847729
Collaborator
(none)
263
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36.3
37.6
1

Study Details

Study Description

Brief Summary

The aim of this study is to determine the current prevalence of co-addictions, including problem/pathological gambling, in patients receiving Opiate Substitution Treatment (OST), and to then compare patients receiving OST with or without a co-addiction (excluding tobacco dependence) in order to determine their clinical profile.

In addition, an ancillary study to be carried out only among those patients receiving methadone, will aim to etablish whether a low plasma concentration of methadone, on the one hand, and an ultrarapid metabolizer genetic profile, on the other, are the characteristics most commonly associated with the presence of co-addictions. This will allow us to complete patient's pharmacological characterization.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Non-interventionel study Total duration: 12 months (preparation, recruitment, analysis) Recruitment period: 6 months Duration of monitoring per patient: no monitoring

    Main objective: to assess the current prevalence of addictive co-morbidities in opiate-dependent subjects receiving Opiate Substitution Treatment (OST) for at least 6 months.

    Secondary objective: to compare patients being treated using OST who currently have a co-addiction (with the exception of tobacco dependence) with patients being treated with OST who do not currently have a co-addiction, based on pharmacological and clinical characteristics (for pharmacological characteristics: pharmacokinetic and pharmacogenetic analyses as part of an ancillary study into only those patients being treated with methadone).

    Main judgment criterion: Presence or absence of co-addictions (except tobacco dependence), determined using assessment tools.

    The secondary assessment criteria shall be: sociodemographic data, data about opiate dependence, data about other substance use disorders, data about gambling practice, psychopathological data (impulsivity, ADHD), pharmacokinetic data and pharmacogenetic data.

    Statistical analysis: For the main judgment criterion, a rate of prevalence of current co-addictions will be estimated using a 95% confidence interval.

    Descriptive analyses will be carried out for all variables gathered and along with point estimates and 95% confidence intervals for qualitative and quantitative variables.

    The second stage will involve univariate exploratory analyses. The two groups of patients will be compared according to the presence or absence of co-addictions. For the quantitative variables Student tests or non parametric tests will be used. For the qualitative variables, we will use Chi-squared or Fisher tests.

    Finally, multivariate analyses will be carried out. The factors that have been previously identified as a being linked to co-addictions (with the threshold p = 0.2) will the be incorporated into logistic regression models. The best model, wich enables explanation of the co-addictions will then be selected using likelihood ratio tests.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    263 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    A Multicenter Study Assessing the Prevalence of Co-addictions in Subjects Receiving Maintenance Treatment for Opiate Dependence. Determination of Clinical and Pharmacological Profil.
    Actual Study Start Date :
    Jul 11, 2013
    Actual Primary Completion Date :
    Jul 21, 2016
    Actual Study Completion Date :
    Jul 21, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    Patients on OST prescribed to treat opiate dependence

    Collecting socio-demographic data, data concerning opiate dependence, data about other substance use disorder, data regarding gambling practice, psychopathological data.

    Outcome Measures

    Primary Outcome Measures

    1. Presence or absence of co-addictions (exept tobacco dependence) [1 day]

      Questionnaire

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    General Inclusion Criteria:
    • Over 18,

    • Under treatment unsing methadone or buprenorhine (+/- naloxone) or morphine as substitute, prescribed for opiate dependence,

    • OST begining at least 6 months previously,

    • Incarceration for less than a month in the event of monitoring in SMPR,

    • Good understanding of French, able to read and write.

    General non-Inclusion Criteria:
    • Protected adults (guardianship, wardship)

    • Disorder of higher-order brains functions (severe cognitive disorders or confusion) or psychotic disorder (hallucinations, delusion) that may interfere with the study.

    Non-Inclusion criteria for patients participating in the ancillary study:
    • Medical monitoring by a doctor from the Drug Addiction Network of the Nantes Area,

    • OST other than methadone

    • Adjustement to dosage in the 5 days prior to administering OST

    • Pregnant women

    • Absence of social security registration.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Brest Universit Hospital Brest France 29820
    2 CSAPA "La métairie" La Roche sur Yon France 85000
    3 Morlaix Hospital Morlaix France 29672
    4 CSAPA "Le triangle" Nantes France 44000
    5 University Hospital Nantes Nantes France 44093
    6 CSAPA-CAARUD "La rose des vents" Saint Nazaire France 44600
    7 Réseau toxicomanie de la région nantaise Saint-Sébastien-sur-Loire France 44230

    Sponsors and Collaborators

    • Nantes University Hospital

    Investigators

    • Study Director: Marie Grall-Bronnec, PH, Nantes University Hospital
    • Principal Investigator: Régis Bouquié, AHU, Nantes University Hospital
    • Principal Investigator: Stéphane Bézieau, Pr, Nantes University Hospital
    • Principal Investigator: Pierre Bodenez, University Hospital, Brest
    • Principal Investigator: Morgane Guillou-Landréat, Morlaix Hospital
    • Principal Investigator: Bertrand Legeay, Medico-psychological regional service nantes University Hospital
    • Principal Investigator: Isabelle Martineau, La Métairie center care support and prevention of addiction
    • Principal Investigator: Philippe Levassor, La Rose des Vents center care support and prevention of addiction
    • Principal Investigator: Jean-Yves Guillet, General practitioners in the drug-addiction network of the Nantes Area

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Nantes University Hospital
    ClinicalTrials.gov Identifier:
    NCT01847729
    Other Study ID Numbers:
    • RC12_0498
    First Posted:
    May 7, 2013
    Last Update Posted:
    Dec 12, 2018
    Last Verified:
    Dec 1, 2018

    Study Results

    No Results Posted as of Dec 12, 2018