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Assessing the Impact of Varenicline on Brain-Behavior Vulnerability

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University of Pennsylvania

Status and phase

Withdrawn
Phase 2

Conditions

Varenicline and the Blunting of Cocaine Cues

Treatments

Drug: chantix

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00895557
Supplement (Other Grant/Funding Number)
1P50DA012756 (U.S. NIH Grant/Contract)
807134
DPMC

Details and patient eligibility

About

Our proposal will enable us to study cocaine patients to determine whether varenicline can weaken brain arousal to drug cues in an fMRI imaging setting, which is what we theorize. This supplement supports a pilot imaging study in cocaine dependence. It will evaluate the impact of varenicline on the brain response to ultra-brief drug and comparison cues in an event-related fMRI paradigm. This is a pilot study.

We will additionally examine the impact of varenicline on addiction-relevant behavioral probes of impulsivity, inhibition, attentional and affective bias. The proposed study will provide the first brain-behavioral probes of varenicline's cocaine-relevant actions in humans, and will provide the critical scientific rationale to move the agent into future collaborative clinical trials.

Sex

Male

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Physically healthy male substance abuse subjects age 18-55.

Exclusion criteria

    1. Participation in clinical trial and receipt of investigational drug(s) during previous 60 days 2) Clinically significant cardiovascular, hematologic, hepatic, renal, neurological or endocrinological abnormalities 3) History of serious head trauma or injury causing loss of consciousness that lasted more than 3 minutes. 4) Presence of magnetically active prosthetics, plates, pins, broken needles, permanent retainer, bullets, etc. in subject's body (unless a radiologist confirms that its presence is unproblematic). A x-ray may be obtained to determine eligibility. 5) Claustrophobia or other medical condition disabling subject from lying in the MRI for approximately 60 minute

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 1 patient group

chantix
Active Comparator group
Treatment:
Drug: chantix

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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