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Active, Not Recruiting

NCT Number: NCT03950492

Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioid Use Disorder

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

21 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

West Virginia University Rockefeller Neuroscience Institute

Morgantown, West Virginia, 26506, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fulfills current DSM-5 (American Psychiatric Association Diagnostic and statistical manual of mental disorders, 5th ed, 2013) diagnostic criteria for OUD (severe) and at least a 5-year history.
  • Participants may have comorbid SUD diagnoses at mild, moderate or severe levels, however OUD must be the primary disorder for which the individual is seeking treatment and the other use disorders must occur in the context of relapse
  • Failed at least two levels of treatment (outpatient/Comprehensive Opioid Addiction Treatment (COAT), intensive outpatient/intensive COAT, residential, inpatient, Adult Intensive Outpatient Program (AIOP), Dual Diagnosis Unit (DDU), which included buprenorphine/naloxone.
  • At least two overdose survivals or one overdose survival and one life-threatening infectious disease complication with relapse after treatment (e.g., endocarditis with valve repair/replacement) within the past 1 year.
  • Family/Social Support/Involvement (as assessed via the Multidimensional Scale of Perceived Social Support).
  • Is able to provide informed consent.

Exclusion criteria

  • Medical problems requiring intensive medical or diagnostic management.
  • Diagnosis of acute myocardial infarction or cardiac arrest within the previous 6 months.
  • History of a neurosurgical ablation procedure.
  • Any medical contraindications to undergoing DBS surgery.
  • History of hemorrhagic stroke.
  • Life expectancy of <3 years
  • Past or present diagnosis of schizophrenia, psychotic disorder, bipolar disorder, or untreated depression other than one determined to be substance induced (assessed via SCID-5). Any treated depression has to have been in remission for one year.
  • Baseline assessment on the Hamilton Depression Rating Scale (HAMD) of greater than 17 or increased risk of suicide based upon any positive response on the Columbia Suicide Severity Scale.
  • Cluster A or B Personality Disorders.
  • Diagnosis of dementia.
  • History of neurological disorder.
  • History of previous neurosurgery (brain) or head trauma.
  • History of suicide attempt.
  • Parental history of completed suicide.
  • Abnormal coagulation lab studies or uncontrolled hypertension.
  • Implanted neurostimulators.
  • Any current CNS infection or infection with the Human Immunodeficiency Virus (HIV).
  • Unable to undergo MR-imaging.
  • Documentation of MRI abnormality indicative of a neurological condition.
  • Substance abuse treatment mandated by court of law.
  • Pregnant or planning to become pregnant.
  • Conditions requiring diathermy.
  • Anticoagulant treatment.
  • Primary language other than English.
  • Any evidence of systemic infection.

Treatment and study plan

Deep Brain Simulator

Device

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.

Primary outcomes

  1. Total Number of Study-Emergent Adverse Events

    Time frame: Enrollment - 52 weeks

    Study participants will be closely monitored for adverse events following DBS surgery with regular check-ups by study personnel.

  2. Change in Opioid Use

    Time frame: 12 weeks

    Opioid use as measured by quantitative urine toxicology via high pressure liquid chromatography.

Secondary outcomes

  1. Participant Survival

    Time frame: 12 -52 weeks

    Incidence of drug overdose deaths among the participants.

  2. Treatment Retention

    Time frame: 12 - 52 weeks

    Participants' retention in traditional medication assisted treatment (MAT).

  3. Incidence of Serious Infectious Disease Complications

    Time frame: 12 - 52 weeks

    Laboratory tests and evaluation to discern presentation of infectious disease.

  4. Mood, Craving and Executive Function

    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.

Other outcomes

  1. Frontal Lobe Metabolism

    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

  2. Changes in Dopamine

    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.

Sponsors and collaborators

Lead sponsor

West Virginia University

Other

Collaborators

  • Medtronic
  • National Institute on Drug Abuse (NIDA)

Registry information

Official study title

Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory

Acronym: DBS_OUD

Important dates

Study start
2019
Primary completion
2022
Study completion
2026
First posted
May 15, 2019
Registry last updated
Jul 28, 2025

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.

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