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Alcohol Dependence clinical trials

View clinical trials related to Alcohol Dependence.

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NCT ID: NCT00572117 Completed - Bipolar Disorder Clinical Trials

Adjunctive Topiramate for Treatment of Alcohol Dependence in Patients With Bipolar Disorder

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is determine whether the use of topiramate is effective in the treatment of alcohol dependence (i.e. decreases drinking) in patients with bipolar disorder.

NCT ID: NCT00571246 Withdrawn - Clinical trials for Post Traumatic Stress Disorder

The Use of Anticonvulsants for Treatment of Patients With Alcohol Dependence and Post Traumatic Stress Disorder

Start date: June 2012
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy of topiramate (250mg) or lamotrigine (250mg) versus placebo in reducing alcohol consumption and decreasing symptoms of PTSD in patients with comorbid AD and PTSD.

NCT ID: NCT00570388 Recruiting - Alcohol Dependence Clinical Trials

Neurocognitive Functioning Following The PROMETA® Treatment Protocol In Subjects With Alcohol Dependence

Start date: March 2007
Phase: N/A
Study type: Interventional

This study will test the safety and efficacy of the PROMETA® Treatment Protocol (which includes the benzodiazepine antagonist flumazenil) in reversing the neurocognitive impairment and this in turn will lead to improved ability to resist alcohol related cues and enhance involvement in psychosocial treatment.

NCT ID: NCT00563797 Completed - Depression Clinical Trials

Mecamylamine for the Treatment of Patients With Depression and Alcohol Dependence

Start date: August 2007
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy of mecamylamine (MEC, 10 mg/day) versus placebo in reducing depressive and alcohol symptoms in patients with depression and co-morbid alcohol dependence. The researchers hypothesize that MEC will significantly reduce depressive symptoms and decrease alcohol consumption compared to placebo in patients with depression and alcohol dependence who are on a stable dose of a selective serotonin reuptake inhibitor (SSRI).

NCT ID: NCT00523133 Completed - Alcohol Dependence Clinical Trials

Research on Individualized Treatment for Alcoholism

RITA
Start date: September 2000
Phase: Phase 2
Study type: Interventional

The purpose of this study was to compare the effects of two psychosocial treatments that differed in scope and intensity (Broad Spectrum Treatment and Motivational Enhancement Treatment) combined with 3 or 6 months of treatment with naltrexone on alcohol drinking behaviors in alcohol dependent patients.

NCT ID: NCT00513708 Completed - Alcohol Dependence Clinical Trials

Facilitating Aftercare for Alcohol Detox Patients

Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether peer visits (known as "12th Step Calls") and professional counselors (using "Motivational Enhancement Therapy") are effective helping alcoholics link to substance abuse treatment programs after being in the hospital for detox.

NCT ID: NCT00511836 Completed - Alcohol Dependence Clinical Trials

ALK21-018: Effects of Medisorb® Naltrexone (VIVITROL®) on Alcohol Craving in Treatment-seeking, Alcohol-dependent Adults

Start date: July 2007
Phase: Phase 4
Study type: Interventional

This was a study of the effects of VIVITROL® on alcohol cue-induced craving and the associated brain activation patterns in alcohol-dependent adults who had recently completed alcohol detoxification and were seeking further treatment for their alcohol dependence. The study was powered to to detect whether VIVITROL attenuates or blocks the BOLD signal increases in response to alcohol-related cues. In the double-blind portion, subjects received a single administration of study drug (VIVITROL 380 mg or placebo). Subjects who completed the double-blind portion could opt to continue to the open-label portion and receive 2 additional months of treatment with VIVITROL 380 mg.

NCT ID: NCT00501631 Completed - Alcohol Dependence Clinical Trials

ALK21-014: Efficacy and Safety of Medisorb® Naltrexone (VIVITROL®) After Enforced Abstinence

Start date: July 2007
Phase: Phase 3
Study type: Interventional

VIVITROL is indicated for the treatment of alcohol dependence in patients who are able to abstain from alcohol in an outpatient setting prior to initiation of treatment with VIVITROL. This Phase 3B trial was designed to evaluate the efficacy and safety of VIVITROL versus placebo. Injections were administered to patients in whom abstinence was enforced by a period of inpatient hospitalization of 7 to 21 days.

NCT ID: NCT00484367 Active, not recruiting - Alcohol Dependence Clinical Trials

A Comparison of Adolescent Group Therapy and Transitional Family Therapy for Adolescent Alcohol and Drug Abusers

Start date: July 1999
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness of two psychosocially-based, manual-driven, behavioral modalities. One of these is a standardized version of the established modality of Adolescent Group Therapy (AGT), which includes both psychoeducational and therapeutic components. The other is a state-of-the-art family therapy approach, Transitional Family Therapy (TFT), which integrates management of the current problem with exploration of multigenerational issues. Both approaches have been developed to expressly target adolescent alcohol problems.

NCT ID: NCT00466661 Completed - Bipolar Disorder Clinical Trials

Acamprosate vs. Placebo in Bipolar Alcoholics

Start date: April 2007
Phase: Phase 4
Study type: Interventional

To conduct a double-blind, randomized, placebo-controlled outpatient clinical trial of acamprosate in individuals with alcohol dependence and bipolar disorder who are also receiving mood stabilizing medication. The study will assess the safety and efficacy of acamprosate in alcohol-dependent bipolar patients as measured by its effects on alcohol use and mood symptoms relative to placebo. The primary hypothesis to be tested is whether individuals with comorbid bipolar disorder and alcohol dependence who receive acamprosate plus mood stabilizer will have greater improvement in alcohol-related outcomes than those who receive mood stabilizer alone. A secondary hypothesis that will be explored is that alcohol-dependent bipolar individuals treated with acamprosate will have greater mood stability as compared to those treated with mood stabilizers alone.