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Recruiting NCT07085377

NCT07085377 Autonomous Methadone Delivery System by Nurses

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Clinical Trial Summary
NCT ID NCT07085377
Status Recruiting
Phase —
Sponsor Hospices Civils de Lyon
Condition Opioid Use Disorder (OUD)
Study Type INTERVENTIONAL
Enrollment 182 participants
Start Date 2025-12-08
Primary Completion 2028-04-08

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
DIADEME strategyControle strategyIndividual semi directive interview

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 182 participants in total. It began in 2025-12-08 with a primary completion date of 2028-04-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Initiations of methadone treatment for opiode use disorder (OUD) are carried out in France in specialized centers, known as centers for care, support and prevention in addictology (CSAPA) In this way, hospital practitioners initiate the prescription of methadone, which is delivered on the spot by the nursing team. CSAPA nurses, and addictology nurses more generally, have a real range of skills which can include adapting treatment doses according to a protocol pre-established in a team, and medically validated (French law no. 2019-774 of July 24, 2019 relating to the organization and transformation of the healthcare system). The methadone speciality used for initiation in CSAPAs is almost always the syrup form. The capsule form can only be used after one year's treatment, unless exceptionally authorized by the medical officer of the French National Health Insurance Fund. However, regulations stipulate that the prescription of methadone syrup must be renewed every fourteen days, which in theory means that a CSAPA doctor must see the patient at least twice a month to renew the prescription, throughout the entire course of treatment. In practice, medical resources are often not sufficient for patients to be seen by a doctor at such a rate. Numerous palliative organizations exist, though they remain poorly described and documented. In some centers, doctors focus primarily on initiations, and prescriptions for patients for whom "stability" has been achieved are sometimes renewed for longer periods than fourteen days, with nurses in charge of assessing whether this organization is suitable for the patient. The notion of stability varies significantly from one center to another, and may mean achieving a constant dose, stopping illicit opioid use, or other criteria more focused on the patient's psychosocial reintegration. By outlining the missions of Addictology nurses, and more specifically of CSAPA nurses, the investigators can define the essential skills required of nurses to carry out these missions. The main hypothesis of the DIADEME study is that semi-autonomous management of methadone treatment initiation by CSAPA nursing teams helps to reinforce adherence to care and thus improve retention rates in the 3 months following initiation.

Eligibility Criteria

Inclusion Criteria: * Subject 18 years of age or older, * With opioid use disorder (OUD) according to DSM-5 (Diagnostic and Statistical Manual of Mental Disorders) criteria (other authorized psychoactive substance use), * Intending to start methadone treatment for OUD in a CSAPA center within 7 days, * Agreeing to be followed up in a CSAPA over the next 3 months, Exclusion Criteria: * Having taken methadone treatment (on prescription) in the three months prior to inclusion, * Simultaneous medical care in another addictology facility, * with a day-hospital project, * Referral to town prescriber or town pharmacy planned and/or requested by patient before 3 month, * Non-stabilized psychiatric disorder or cognitive impairment likely to compromise compliance and involvement in care (at investigator's discretion), * Inability to communicate and express themselves in French language, * Subject to a legal protection measure other than curatorship, * Pregnant or breast-feeding.

Contact & Investigator

Central Contact

Benjamin ROLLAND, MD

✉ Benjamin.rolland@chu-lyon.fr

📞 4 37 915 072

Frequently Asked Questions

Who can join the NCT07085377 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Opioid Use Disorder (OUD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07085377 currently recruiting?

Yes, NCT07085377 is actively recruiting participants. Contact the research team at Benjamin.rolland@chu-lyon.fr for enrollment information.

Where is the NCT07085377 trial being conducted?

This trial is being conducted at Bayonne, France, Bordeaux, France, Brioude, France, Le Puy-en-Velay, France and 4 additional locations.

Who is sponsoring the NCT07085377 clinical trial?

NCT07085377 is sponsored by Hospices Civils de Lyon. The trial plans to enroll 182 participants.

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