About this trial
The US is suffering from a national opioid epidemic characterized by significant costs, overdoses, and deaths. Conventional Opioid Use Disorder (OUD) treatments (i.e., pharmacological and psychosocial interventions) are characterized by limited or diminishing efficacy, ceiling effects, and/or serious side effects. The availability of validated OUD biomarkers would be a key step in the development and approval of better treatments. Ultimately, the scarcity of OUD biomarkers represents a significant unmet need in the fight against opioid addiction as recognized by NIDA and the FDA with their support for development of Medical Device Development Tools (MDDT) and biomarker tests for OUD. Advances in neuroimaging techniques, and in particular recent evidence supports electroencephalography (EEG) as a promising candidate to investigate the correlation between addiction and brain state. To address the clear medical and market need for OUD biomarkers, this is a feasibility study to identify and assess potential EEG biomarkers for OUD diagnoses, disease monitoring, and prediction of OUD treatment response.
Eligibility criteria
Qualifiers
Providing informed consent to participate in the study.
22 to 85 years old.
Providing informed consent to participate in the study.
22 to 85 years old.
Disqualifiers
Recently started on antiepileptic drug therapy.
Ingestion of poppy seeds or herbal teas containing Papaveris fructus (may cause a positive opiate test for morphine, codeine [72,73]).
History of neurological disorders involving stroke, brain tumors, or epilepsy as self- reported.
History of unexplained fainting spells as self-reported.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
University of Illinois at Chicago
Lead sponsor
National Institute on Drug Abuse (NIDA)
Collaborator