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Study identifier: NCT06642181 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Combined Guanfacine and Mindfulness Meditation as an Adjunct to Buprenorphine Maintenance in Opioid Use Disorder

Condition: Mindfulness · Guanfacine · Opioid Use Disorder  ·  Sponsor: Rutgers, The State University of New Jersey

PhasePhase 1
Planned participants224
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersNo

About this study

The US is currently going through an opioid crisis, and while Medication Assisted Treatments such as buprenorphine (BUP) have proved highly effective at stabilizing the neurobiology underlying acute withdrawal, they have been less effective at preventing longer-term relapse and adherence. This may be due to the fact that they do not fully engage the neural processes sub-serving the emotional control of sensitized negative mood and reward sensitivity during stress- and opioid-cue provocation, respectively. In contrast while the alpha2 agonist, guanfacine, may attenuate stress-provoked opioid craving by mediating top-down prefrontal control over sensitized dysphoria, the behavioral intervention, Mindfulness Oriented Recovery Enhancement (MORE) may reduce opioid cue-provoked craving by mediating top-down prefrontal control over hedonic dysregulation. Furthermore, while both interventions separately may prove effective as longer-term adjunctive therapies, they may offer greater efficacy together, providing a unique medication/behavioral combination able to target both stress and reward provocation mechanisms. To optimally test this hypothesis, a staged approach is proposed to first confirm the efficacy of both GXR and MORE, independently and combined (R61), prior to elucidating underlying neural mechanisms (R33). Using a 2 X 2 design, N=80 OUD individuals on BUP will be randomized to either 6-weeks of Guanfacine extended release (GXR; 3mgs, n=40) or placebo (PBO; n=40). Half of a…

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

Talk to the study team

Suchismita Ray, PhD  ·  732-266-4553  ·  shmita@rutgers.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Rutgers School of Health ProfessionsNewark, New Jersey, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06642181