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| Sponsor: | Forest Laboratories |
|---|---|
| Collaborator: |
National Institute on Drug Abuse (NIDA) |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00360594 |
Purpose
Acamprosate is approved by the Food and Drug Administration (FDA) for the treatment of alcoholism. The purpose of this study is to see if initiating acamprosate early in alcohol detoxification instead of waiting until detoxification has been completed effects the course of detoxification, adverse events during detoxification, drop out rate during the rehabilitative treatment phase, or overall efficacy of acamprosate for those with alcohol dependence who plan to receive at least two months of rehabilitative pharmacotherapy with acamprosate.
| Condition | Intervention | Phase |
|---|---|---|
|
Alcohol Use Disorder |
Drug: Acamprosate Drug: Placebo |
Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Initiating Acamprosate Within Versus Post-detoxification in the Rehabilitative Treatment of Alcohol Dependence. |
| Enrollment: | 40 |
| Study Start Date: | October 2006 |
| Study Completion Date: | November 2007 |
| Primary Completion Date: | September 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Acamprosate
|
Drug: Acamprosate
3 pills (666 mg) for 1998mg/day
Other Name: Campral
|
|
Placebo Comparator: 2
Placebo
|
Drug: Placebo
3 pills (666mg) for 1998mg/day
|
Biphasic clinical trial, consisting of a randomized, double-blind, placebo-controlled detoxification treatment phase (DP), followed by 9-week open-label rehabilitative treatment phase (RP).
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria for Detoxification Treatment Phase
Exclusion Criteria for Detoxification Treatment Phase (DP)
Inclusion Criteria for Post-Detoxification Rehabilitative Treatment Phase (RP/Phase 2) with Open-Label Acamprosate
Contacts and Locations| United States, Pennsylvania | |
| Treatment Research Center | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| Principal Investigator: | Helen Pettinati, Ph.D. | University of Pennsylvania |
More Information
| Responsible Party: | Helen Pettinati, Ph.D., University of Pennsylvania Treatment Research Cener |
| ClinicalTrials.gov Identifier: | NCT00360594 History of Changes |
| Other Study ID Numbers: | 804481, P50DA012756-07, CMP-MD-08, DPMC |
| Study First Received: | August 2, 2006 |
| Last Updated: | December 2, 2009 |
| Health Authority: | United States: Food and Drug Administration; United States: Federal Government |
|
alcoholism |
|
Alcohol Drinking Drinking Behavior Acamprosate Alcohol Deterrents |
Central Nervous System Agents Therapeutic Uses Pharmacologic Actions |