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| Sponsored by: |
Forest Laboratories |
|---|---|
| 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: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment |
| 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 |
|---|---|
|
1: Experimental
Acamprosate
|
Drug: Acamprosate
3 pills (666 mg) for 1998mg/day
|
|
2: Placebo Comparator
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 Detoxication Treatment Phase
Exclusion Criteria for Detoxication Treatment Phase (DP)
Female Subjects who are pregnant or lactating, or female Subjects of child bearing potential who are not using acceptable methods of birth control.
Acceptable methods of birth control include: tubal ligation, barrier (diaphragm or condom) with spermicide, intrauterine progesterone contraceptive system, levonorgestrel implant, medroxyprogesterone acetate contraceptive injection, and oral contraceptives.
Clinical laboratory tests (CBC, blood chemistries, urinalysis) outside normal limits that are clinically unacceptable to the Principal Investigator.
EKG1st degree heart block, sinus tachycardia, left axis deviation, and nonspecific ST or T wave changes are allowed; liver function tests [LFTs] <5 x ULN are acceptable), Subjects with impaired renal function as indicated by corrected creatinine clearance below 80 ml/min/70 kg as determined by the modified Cockcroft equation (CDC, 1986).
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: | University of Pennsylvania Treatment Research Cener ( Helen Pettinati, Ph.D. ) |
| Study ID Numbers: | 804481, 5 P50 DA012756-07, CMP-MD-08 |
| Study First Received: | August 2, 2006 |
| Last Updated: | December 10, 2008 |
| ClinicalTrials.gov Identifier: | NCT00360594 History of Changes |
| Health Authority: | United States: Food and Drug Administration; United States: Federal Government |
|
alcoholism |
|
Alcoholism Alcohol Drinking Acamprosate Ethanol |
|
Therapeutic Uses Central Nervous System Agents Pharmacologic Actions Alcohol Deterrents Acamprosate |