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Cocaine-Related Disorders clinical trials

View clinical trials related to Cocaine-Related Disorders.

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NCT ID: NCT01601730 Completed - Substance Abuse Clinical Trials

Modafinil - Escitalopram Study for Cocaine Dependence

Start date: August 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to improve the efficacy of modafinil as a potential treatment for cocaine dependence.

NCT ID: NCT01573273 Completed - Cocaine Dependence Clinical Trials

Oxytocin in Cocaine Dependence

Start date: October 2012
Phase: N/A
Study type: Interventional

Stress is likely involved in relapse to cocaine use. This project will investigate the role oxytocin may play in the stress response in cocaine-dependent men and women and examine how oxytocin may impact brain activity in individuals exposed to cocaine-related cues.

NCT ID: NCT01558973 Completed - Alcoholism Clinical Trials

FMRI of Stress and Addictive Disorders

Start date: August 2005
Phase: N/A
Study type: Observational

The purpose of this study is to explore whether frontal brain activation in response to stress varies as a function of the presence or extent of early trauma and whether or not this effect is greater in women compared to men. To examine the effect of stress on thinking and remembering. To examine the separate and interactive effects of stress, addiction, withdrawal, and genetics; and to examine fMRI brain activation associated with stressful, reward-related-cue and neutral/relaxing audiotaped scripts,visual images and emotional video clips in addicted individuals and in healthy controls.

NCT ID: NCT01535573 Completed - Cocaine Dependence Clinical Trials

Citalopram for Cocaine Dependence

Start date: December 2010
Phase: Phase 2
Study type: Interventional

This is a phase 2 clinical trial of citalopram pharmacotherapy for treatment of cocaine dependence. Using a double-blind, randomized controlled design, eligible cocaine dependent patients will be assigned equally to one of three medication conditions: placebo or the Selective serotonin re-uptake inhibitor (SSRI) agent, citalopram at either 20 mg per day or 40 mg per day. It is hypothesized that citalopram will reduce cocaine use and increase periods of sustained abstinence substantially more than placebo. Performance on a set of behavioral tasks of impulsivity will be analyzed as potential predictors of treatment response.

NCT ID: NCT01526538 Completed - Clinical trials for COCAINE-RELATED DISORDERS

Improving Learning-based Treatment of Cocaine Dependence With Medication

Start date: September 2011
Phase: Phase 2
Study type: Interventional

This study will test the efficacy of d-cycloserine in enhancing response to learning-based treatment for cocaine dependence, specifically contingency management.

NCT ID: NCT01486810 Completed - Cocaine Dependence Clinical Trials

Open-Label Pilot Study of Lisdexamfetamine for Cocaine Dependence

Vyvance
Start date: December 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The proposed protocol is an open-label pilot study of the treatment of cocaine dependence using lisdexamfetamine (LDX), a prodrug of d-amphetamine. The investigators plan to enroll 12 patients in an eight-week open-label trial to obtain preliminary data regarding the safety, tolerability, and potential utility of lisdexamfetamine for treatment of cocaine dependence and to determine an effective dosage range.

NCT ID: NCT01468012 Completed - Cocaine Dependence Clinical Trials

Imaging the Neurobiology of Behavioral and Medication Treatment for Cocaine Dependence

COST
Start date: July 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The proposed study will look at cocaine dependent individuals and will consist of three consecutive phases: 1) the 2-week outpatient lead-in phase during which behavioral therapy will be administered; 2) the 15-21 day inpatient phase (during which participants will start study medication of levodopa,carbidopa and entacapone (LCE) and will undergo brain imaging and 3) the 24 weeks outpatient treatment trial. The purpose is to see if treatment with LCE may reverse baseline brain deficits and if this change is associated with clinical improvement. Hypothesis is that treatment with LCE, compared to placebo, increases abstinence from cocaine over a 12-week trial in combination with behavioral treatment with voucher incentives.

NCT ID: NCT01437293 Completed - Cocaine Abuse Clinical Trials

Behavioral and Physiological Effects of Cocaine in Cocaine-dependent Participants Treated With Levodopa in Combination With Carbidopa and Entacapone (LCE)

COST
Start date: August 2010
Phase: Phase 1
Study type: Interventional

An inpatient safety study to characterize the cardiovascular and behavioral effects of cocaine administration in the presence of LCE. The proposed study involves an inpatient stay of 12 days during which participants will have two cocaine-administration sessions, each including five doses of smoked cocaine with ascending doses.

NCT ID: NCT01402492 Completed - Cocaine Dependence Clinical Trials

Cocaine Use Reduction With Buprenorphine

CURB
Start date: September 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to investigate the safety and effectiveness of buprenorphine in the presence of naltrexone for the treatment of cocaine dependence.

NCT ID: NCT01401270 Completed - Cocaine Abuse Clinical Trials

Prize Contingency Management for Cocaine-Dependent Methadone Patients

Start date: November 2011
Phase: N/A
Study type: Interventional

The investigators will randomize 300 cocaine-dependent methadone patients to 1 of 6 conditions: (a) a control group, (b) a contingency management condition that arranges a 100% probability of winning a prize with each draw and has 3 prize categories, (c) a contingency management condition that arranges a 31% probability of winning and has 3 prize categories, (d) a contingency management condition that arranges a 100% probability of winning and has 7 prize categories, (e) a contingency management condition that arranges a 31% probability of winning and has 7 prize categories, or (f) usual prize contingency management with a 50% probability of winning from 3 prize categories. Magnitudes of reinforcement will be identical across conditions, but lower overall probability conditions arrange for greater chances of winning larger magnitude prizes. The investigators expect that the new contingency management conditions will reduce cocaine use relative to the control condition, that 31% probability conditions will decrease drug use relative to 100% conditions, and that 7-prize category conditions will reduce drug use compared to 3-prize category conditions. In addition, the 31%/7-category condition is expected to be most efficacious. Results will be instrumental for further developing prize contingency management to improve outcomes of cocaine-dependent methadone patients.