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Study details
Enrolling now

Individualized Adaptive Deep Brain Stimulation for Opioid Use Disorder

University of California, San Francisco
NCT IDNCT07214467ClinicalTrials.gov data as of Apr 2026
Target enrollment

6

Study length

about 6.1 years

Ages

22–75

Locations

1 site in CA

About this study

Researchers are testing whether personalized (adaptive) Deep Brain Stimulation (DBS) can help reduce cravings and opioid use in people with opioid use disorder. The trial will involve a device that is implanted to stimulate specific areas of the brain.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Use Deep Brain Stimulation
Primary goalIncidence of adverse events during aDBS phase

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Incidence of adverse events during aDBS phase, Incidence of adverse events during sEEG phase

Devices

implantable

Body systems

Psychiatry / Mental Health