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On-site Evaluation of Substances Consumption on Opiate Maintenance (ESUB-MG)

Primary Purpose

Opiate Addiction

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
urine drug testing
no test
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Opiate Addiction focused on measuring Substances consumption, Opiate, Family practice

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA

  • For GPs:Professional criteria: to practice as a GP, to be in activity, to practice in general ambulatory practice (in a medical office), to regularly manage patients treated with buprenorphine, to be registered in sector 1, consent for participating to the study
  • For patients:

Aged 18 years-old or more, to consult for starting buprenorphine or OMT:

  • any patient previously treated by buprenorphine or buprenorphine-naloxone but with his/her treatment interrupted for at least 2 months will be considered as a candidate for a new treatment with buprenorphine or buprenorphine-naloxone
  • any patient previously exposed to opiate maintenance drug obtained illegally "in the street" will not be as treated affiliated to a health insurance scheme, not opposed to participate

EXCLUSION CRITERIA

- For patients: to consult for continuing buprenorphine or for another complain related, to opiate substitution treatment, to be known and yet managed by the GP for an opiate substitutive treatment, to have started buprenorphine in a specialized centre or in a hospital, to be treated with methadone, to be treated with methadone and asking a switch toward buprenorphine

Sites / Locations

  • Clermont-Ferrand Hospital
  • Grenoble Lyon Hospital
  • Marseille Hospital
  • Nancy Hospital
  • Service de Pharmacologie Médicale et Clinique - Centre d'addictovigilance - CHU de Toulouse

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Urine Drug Testing

No test

Arm Description

GPs of the intervention group will dedicate an average 5 minutes during the consult to perform OS-UDT. Patients will be asked to collect a urine sample at the GP's medical office. GP will read and communicate the results immediately to the patients. GPs will keep free of their management according to OS-UDT results.

Patients will not have to performed the OS-UDT test

Outcomes

Primary Outcome Measures

Impact of on-site urine drug screening tests
The main objective will be to assess the impact of on-site urine drug screening tests in general practice compared to routine medical care on OMT retention at six months in opioid-dependent patients initiating buprenorphine.

Secondary Outcome Measures

Acceptability of OS-UDT (One-site Urine Drug Testing) by patients and GPs
To assess if patients and GPs accept to performed the One-Site Urine Drug Testing
Patient's adherence to buprenorphine (duration and dose)
General Practitioner will assessed if patients follow their treatments (duration and dose)
Associated consumptions (decrease in using psychoactive substances)
GP will assessed and characterized other medical products taken in association with the treatment studied.

Full Information

First Posted
May 14, 2014
Last Updated
February 28, 2022
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT02345655
Brief Title
On-site Evaluation of Substances Consumption on Opiate Maintenance
Acronym
ESUB-MG
Official Title
Impact of On-site Evaluation of Substances Consumption on Opiate Maintenance in the Context of Family Practice
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
April 11, 2016 (Actual)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In France, General Practitioners (GPs) are widely involved in opiate maintenance treatment (OMT) by initially prescribing buprenorphine and monitoring patients under buprenorphine and methadone. Number of treated patients is around 150,000 with 75% of them treated by buprenorphine. Among the guidelines for improving OMT, urine testing is mandatory for initiating methadone, whereas it is recommended for initiating buprenorphine and during follow-up. Urine drug tests are based on immunoassay techniques and enable a qualitative analysis of the recent drug consumption, with detection based on designated thresholds, allow a better appraisal of drug exposure, before initiating and during OMT. While intrinsic diagnostic value of these tests is already demonstrated, the consequences of carrying out these tests on OMT have not been clearly established. Some studies suggest that patients exposed to drug tests may have a better OMT retention and in patients treated by methadone, performing urine screening tests has been shown to be associated with a mortality risk reduction in a Scottish retrospective cohort of opioid addicts. Actually, despite the recommendations to perform these tests, few GP prescribe tests, and few patients are regularly screened. Availability of commercial kits for urine drug testing in the medical office should improve their utilisation. The widespread of urine drug screening tests use in ambulatory care is a reality for some GPs working in addictology networks. Despite a global benefit reported in the literature with a better control in prescribing OMT and a better patients' adherence, as far as the investigators know, no study has yet explored the impact of the use of urine drug screening test in decision making in general practice with an intervention study.
Detailed Description
In a retrospective cohort study of methadone users performed through data obtained from a primary care prescription registry in Tayside, Scotland, McCowan et al examined the interaction of patient related factors and prescribing factors at the individual level and assess their independent impact on the risk of both all-cause mortality and drug dependent cause specific mortality (McCowan, Kidd et al. 2009). Overall, 181 (8%) people died among 2378 subjects with a median follow-up of 4.38 years. Overuse of methadone, history of psychiatric admission, and increasing comorbidity were all associated with an increase in all-cause mortality. Longer duration of use (adjusted hazard ratio 0.95, 0.94 to 0.96), history of having urine tested (0.33, 0.22 to 0.49), and increasing time since last filled prescription were protective in relation to all-cause mortality. These factors are likely to be markers of people who are stabilised on maintenance treatment and engaged in monitoring procedures or who have successfully completed a methadone treatment reduction programme. This community based study gives a clear indication of the prescribing, monitoring, and management of patients in OMT and the subsequent impact on all cause and drug dependent mortality. This study provides evidence that recommendations on best practice (including specifically performing UDS) improve patients' outcomes. Using data from the French "Methaville" trial, Roux et al (Roux, Michel et al. 2012; Roux, Lions et al. 2013) investigated the effect of pre-treatment and in-treatment factors on long-term non-adherence to this OMT. Four pre-treatment predictors of non-adherence were identified: being female, not having stable housing, alcohol consumption and cocaine use. These findings highlight the need to appropriately assess psychoactive drug use when starting OMT, and urine drug testing should be consider as a way to reach this aim. On the basis of the literature, one would suppose that carrying out UDS would provide an improvement in the management of patients with abuse or addiction and would be helpful, particularly in community office-based settings, as office-based management of opioid dependence grows up (Walley, Alperen et al. 2008). Despite the lack of significant evidence of efficacy, UDS are recommended to assess the use of psychoactive substances when abuse or addiction is suspected.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opiate Addiction
Keywords
Substances consumption, Opiate, Family practice

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Urine Drug Testing
Arm Type
Experimental
Arm Description
GPs of the intervention group will dedicate an average 5 minutes during the consult to perform OS-UDT. Patients will be asked to collect a urine sample at the GP's medical office. GP will read and communicate the results immediately to the patients. GPs will keep free of their management according to OS-UDT results.
Arm Title
No test
Arm Type
Other
Arm Description
Patients will not have to performed the OS-UDT test
Intervention Type
Procedure
Intervention Name(s)
urine drug testing
Intervention Description
Performed a OS-UDT test in general practice on patients starting buprenorphine
Intervention Type
Other
Intervention Name(s)
no test
Intervention Description
normal procedure decided by the general practitioner
Primary Outcome Measure Information:
Title
Impact of on-site urine drug screening tests
Description
The main objective will be to assess the impact of on-site urine drug screening tests in general practice compared to routine medical care on OMT retention at six months in opioid-dependent patients initiating buprenorphine.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Acceptability of OS-UDT (One-site Urine Drug Testing) by patients and GPs
Description
To assess if patients and GPs accept to performed the One-Site Urine Drug Testing
Time Frame
6 months
Title
Patient's adherence to buprenorphine (duration and dose)
Description
General Practitioner will assessed if patients follow their treatments (duration and dose)
Time Frame
6 months
Title
Associated consumptions (decrease in using psychoactive substances)
Description
GP will assessed and characterized other medical products taken in association with the treatment studied.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA For GPs:Professional criteria: to practice as a GP, to be in activity, to practice in general ambulatory practice (in a medical office), to regularly manage patients treated with buprenorphine, to be registered in sector 1, consent for participating to the study For patients: Aged 18 years-old or more, to consult for starting buprenorphine or OMT: any patient previously treated by buprenorphine or buprenorphine-naloxone but with his/her treatment interrupted for at least 2 months will be considered as a candidate for a new treatment with buprenorphine or buprenorphine-naloxone any patient previously exposed to opiate maintenance drug obtained illegally "in the street" will not be as treated affiliated to a health insurance scheme, not opposed to participate EXCLUSION CRITERIA - For patients: to consult for continuing buprenorphine or for another complain related, to opiate substitution treatment, to be known and yet managed by the GP for an opiate substitutive treatment, to have started buprenorphine in a specialized centre or in a hospital, to be treated with methadone, to be treated with methadone and asking a switch toward buprenorphine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maryse LAPEYRE-MESTRE, MD
Organizational Affiliation
University Hospital of Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clermont-Ferrand Hospital
City
Clermont-Ferrand
Country
France
Facility Name
Grenoble Lyon Hospital
City
Grenoble
Country
France
Facility Name
Marseille Hospital
City
Marseille
Country
France
Facility Name
Nancy Hospital
City
Nancy
Country
France
Facility Name
Service de Pharmacologie Médicale et Clinique - Centre d'addictovigilance - CHU de Toulouse
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26931763
Citation
ESUB-MG Study Group. Study protocol of the ESUB-MG cluster randomized trial: a pragmatic trial assessing the implementation of urine drug screening in general practice for buprenorphine maintained patients. BMC Fam Pract. 2016 Mar 1;17:24. doi: 10.1186/s12875-016-0413-3.
Results Reference
derived

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On-site Evaluation of Substances Consumption on Opiate Maintenance

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