Pilot Study of a Multi-System Analysis of Opioid Receptor Binding
Study of Opioid Receptor Binding in Individuals with and without a History of Opioid Misuse
Brief description of study
- Cohort 1: Subjects with a lifetime diagnosis of Opioid Use
Disorder (OUD) on a stable dosage of buprenorphine or methadone for medication-assisted
treatment (MAT) for at least four weeks prior to the screening visit
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Cohort 2:
Subjects with a lifetime history of OUD, but not current OUD who have not received MAT for OUD
during the 12 months prior to screening
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Cohort
3: Subjects without a lifetime history
of OUD
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Healthy Controls,Opioid Use Disorder,History of Opioid Use Disorder,Opiate use,Opioid Use
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Age: 18 years - 50 years
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Gender: All
This study investigates opioid receptor binding in the brain and body. It aims to understand how these receptors, which are involved in pain reduction and reward experiences, function in different individuals.
The study focuses on measuring the binding of a specific type of opioid receptor using a PET/CT scan. This involves a special imaging drug that helps visualize these receptors in the body.
- Who can participate: Up to 60 adults will be enrolled, divided into three groups: those with a history of Opioid Use Disorder (OUD) on treatment, those with a history of OUD not on treatment, and those without a history of OUD.
- Study details: Participants will undergo PET/CT scans to measure opioid receptor binding. The imaging drug used, [11C]carfentanil, is investigational and approved for research use only.
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