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Study identifier: NCT05886582 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Transdermal Rotigotine as Adjunct to Behavioral Therapy for Cocaine Use Disorder

Condition: Substance-Related Disorders  ·  Sponsor: Virginia Commonwealth University

PhasePhase 2
Planned participants40
Who can joinAll sexes, 25 Years to 70 Years
Healthy volunteersNo

About this study

This is a randomized, double-blind, placebo-controlled phase 2b pilot clinical trial to determine whether non-ergoline D3/D2/D1 dopamine (DA) receptor agonist rotigotine (RTG), in combination with treatment as usual, including individual or group behavioral therapy can a) reduce cocaine use and also b) increase brain activity in frontocortical areas of the brain, and, as a reflection of that - improve top-down cognitive control in persons with cocaine use disorder (CocUD). Rotigotine is a marketed non-ergoline D3/D2/D1 DA agonist (RTG, Neupro®) in the form of a transdermal patch that is FDA-approved for the treatment of Parkinson's Disease and Restless Legs Syndrome. The premise of this project was based on apparent beneficial effects of RTG in a different human population characterized by executive function (EF) impairment. In light of the deficits in EF common in persons with CocUD, RTG may hold the potential for cognitive improvement in persons with CocUD who are in treatment as usual to both attend to and retain psychoeducation concepts better. In addition, rotigotine may help these individuals in recovery maintain goals better, where goal maintenance is a crucial integrative product of successful EF.

This description comes directly from the study's public registry record.

Talk to the study team

Tiffany Pignatello, FNP  ·  (804) 827-3784  ·  study4u@vcu.edu

Lori Keyser-Marcus, PhD  ·  804-828-3686  ·  study4u@vcu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Virginia Commonwealth UniversityRichmond, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05886582