Evaluating a Novel Medication Device for Methadone Dosing
Completed · Not applicable
Conditions studied: Opioid-use Disorder
In brief
This study will evaluate whether a commercially available, secure, electronic pill box is a feasible, acceptable, and satisfactory method to manage take-home dosing of methadone for both methadone clinic patients and staff members.
Key facts
- Study ID
- NCT03254043
- Run by
- Johns Hopkins University
- People needed
- 26
- Starts
- 2018-01-31
- Expected to finish
- 2020-03-30
- Last updated by the study team
- 2020-09-28
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years or older
- Receiving methadone for the treatment of opioid use disorder for at least 90 days and having been on the same methadone dose for at least 30 days
- Have previously received a take-home dose of methadone as part of routine care
- Be willing to comply with the study schedule
- Be a methadone patient in the clinic within which this study is being conducted
You may not qualify if…
- Pregnancy
- Presence of an acute medical problems that requires immediate or intense medical management
- Presence of serious or unstable mental illness that interferes with study procedures
- Planning to leave methadone treatment within the next 12 weeks
- Being maintained on a dose of methadone that is less than 10mg or more than 100mg
- Currently receiving split doses of methadone as part of routine care
Where it is running
- Addiction Treatment Services (ATS) — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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