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Cocaine Abuse clinical trials

View clinical trials related to Cocaine Abuse.

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NCT ID: NCT03971097 Completed - Clinical trials for Alcohol Use Disorder

The Effect of Self-Forgiveness on Self-Stigma in Addiction.

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

This study has an experimental design and will examine the difference in pre-test and post-test data on the Self-Forgiveness Dual Process Scale (SFDPS) (Griffin, Worthington, Davis, Hook, & Maguen, 2018) and the Substance Abuse Self-Stigma Scale (SASSS) (Luoma et al., 2013). Data will be collected from two groups of participants receiving counseling at the short-term rehabilitation facility located at University of Pittsburgh Medical Center's (UPMC). Individuals who agree to participate in the study will be randomly assigned to either the experimental group (EG) or the control group (CG). Data collected will include pre-test SFDPS and SASSS scores for the EG and the CG (collected within 24-hours of admission), and post-test SFDPS and SASSS scores for the EG and CG (collected after 14 days). ANCOVA will be used to analyze the pre-test and post-test data recorded from participants' scores.

NCT ID: NCT02563769 Completed - Cocaine Dependence Clinical Trials

Clavulanic Acid (CLAV) and Cocaine Interaction Safety Study

Start date: October 24, 2016
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine if it is safe to use the study drug, clavulanic acid, in combination with cocaine. In this study, subjects will receive intravenous (i.v.) cocaine and the study drug, clavulanic acid. The safety of clavulanic acid is being studied so future studies can be done to find out if this drug is helpful in treating cocaine dependence. Currently, there is no available medication treatment for cocaine dependence.

NCT ID: NCT02393599 Completed - Cocaine Abuse Clinical Trials

Study to Assess Potential Interactions Between Intravenous Cocaine and Oral Lorcaserin

Start date: May 2015
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to determine if there are significant interactions between oral lorcaserin treatment concurrent with 20 and 40 mg intravenous (i.v.) cocaine infusions by measuring adverse events (AEs) and cardiovascular responses including heart rate (HR), blood pressure (BP), and electrocardiogram (ECG) (including QTc).

NCT ID: NCT02141620 Completed - Cocaine Dependence Clinical Trials

n-Acetylcysteine and Cocaine

Start date: May 2014
Phase: Phase 0
Study type: Interventional

This study will determine the initial efficacy, safety and tolerability of n-acetylcysteine as a pharmacotherapy for cocaine dependence. A rigorous, inpatient human laboratory study will be conducted in which the subjective, physiological and reinforcing effects of cocaine are evaluated during maintenance on placebo and n-acetylcysteine.

NCT ID: NCT01651377 Completed - Substance Abuse Clinical Trials

Pramipexole as a Treatment for Cocaine Dependence

Start date: October 2011
Phase: Phase 1
Study type: Interventional

The purposes of this study are as follows: 1. To assess the cardiovascular and subjective effects of cocaine during treatment with pramipexole and placebo. 2. To assess the reinforcing effects of cocaine, measured using choice procedures, during treatment with pramipexole and placebo.

NCT ID: NCT01651364 Completed - Substance Abuse Clinical Trials

A Pilot Study of Cabergoline for the Treatment of Cocaine Dependence

Start date: July 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effects of treatment with cabergoline, compared to treatment with placebo, on cocaine induced craving and subjective effects in cocaine-dependent human volunteers.

NCT ID: NCT01601743 Completed - Substance Abuse Clinical Trials

Exercise as a Behavioral Treatment for Cocaine Dependence

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

The purpose of this study is to test the effects of exercise on cocaine use, fitness, and cravings for cocaine and nicotine. This study is part of an effort to develop treatments for cocaine abuse.

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: 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: 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.