West Virginia University Rockefeller Neuroscience Institute
Morgantown, West Virginia, 26506, United States
NCT Number: NCT03950492
The purpose of this clinical study is to investigate the safety, tolerability, and feasibility of Deep Brain Stimulation (DBS) of the nucleus accumbens (NAc) and ventral internal capsule (VC) for participants with treatment refractory opioid use disorder (OUD) who have cognitive, behavioral, and functional disability. This study will also provide critical information for planning subsequent clinical trials.
This study is active but is not currently recruiting participants.
21 year–50 year
All sexes
Interventional
Not applicable
Morgantown, West Virginia, 26506, United States
The overarching goal of this study is to evaluate the safety, tolerability, feasibility and impact on outcomes of NAc/VC DBS for treatment refractory OUD. In treatment refractory OUD, innovative approaches and more invasive interventions including DBS are warranted to improve outcomes.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This is an open-label, safety, tolerability, and feasibility study for participants who have treatment refractory OUD that are eligible to have DBS targeting the NAc/VC.
Time frame: Enrollment - 52 weeks
Study participants will be closely monitored for adverse events following DBS surgery with regular check-ups by study personnel.
Time frame: 12 weeks
Opioid use as measured by quantitative urine toxicology via high pressure liquid chromatography.
Time frame: 12 -52 weeks
Incidence of drug overdose deaths among the participants.
Time frame: 12 - 52 weeks
Participants' retention in traditional medication assisted treatment (MAT).
Time frame: 12 - 52 weeks
Laboratory tests and evaluation to discern presentation of infectious disease.
Time frame: 12 and 24 weeks post surgery
Participants will complete standardized measures of mood, drug craving, and executive function at 12 weeks and 24 weeks post DBS titration.
Time frame: 3 weeks and 12 weeks post surgery
18fluoro-Deoxy-Glucose (FDG) PET will be use to determine if there is an increase in frontal lobe metabolism following DBS
Time frame: 3 weeks and 12 weeks post surgery
C11 Raclopride PET may be used to examine for changes in dopamine at 12 weeks post titration.
West Virginia University
Other
Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory
Acronym: DBS_OUD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05657106
Acquired Immunodeficiency Syndrome, Blood-Borne Infections
Lexington, Kentucky, United States
View Trial DetailsNCT05141266
Chemically-Induced Disorders, Mental Disorders
Salt Lake City, Utah, United States
View Trial DetailsNCT05603702
Chemically-Induced Disorders, Chronic Abdominal Pain
Stanford, California, United States
View Trial DetailsNCT06810076
Chemically-Induced Disorders, Drug Misuse
Gainesville, Florida, United States
View Trial Details