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Clinical Trial Summary

The investigators will evaluate the effects of an accelerated Transcranial Magnetic Stimulation (TMS) protocol of the left dorsolateral prefrontal cortex (DLPFC) for moderate to severe methamphetamine use disorder. This is a randomized parallel group design to assess feasibility and safety, evaluate efficacy (use, craving) and identify magnetic resonance imaging (resting state and cue craving) associated with group/outcomes.


Clinical Trial Description

In a randomized double-blind parallel-group sham-controlled design (n=20) administer a 5-day accelerated iTBS protocol (40 treatments) to the left dorsolateral prefrontal cortex during a short inpatient stay. Magnetic resonance imaging will be completed pre-post TMS and participants will be followed for 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06320366
Study type Interventional
Source University of Colorado, Denver
Contact Joseph T Sakai, MD
Phone 303-724-7402
Email joseph.sakai@cuanschtz.edu
Status Not yet recruiting
Phase N/A
Start date May 1, 2024
Completion date May 31, 2028

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