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Effectiveness of Tiagabine for Cocaine Dependence in Methadone-Maintained Individual

 
By snjadmin at Fri, 2005-09-02 20:15 | Cocaine | Research

Many opioid-dependent individuals are also dependent on cocaine. Methadone is a widely used and effective method for treating opioid dependence. However, it is not effective in treating other drugs of abuse. The purpose of this study is to determine the effectiveness of another drug, tiagabine, for treating cocaine dependence in opioid-dependent individuals already receiving methadone treatment.

Study start: December 2004

For over 30 years, methadone has been used to treat opioid addiction. Since methadone is effective in reducing withdrawl symptoms, it is used as a method of detoxification for opiate addicts. However, methadone is not effective in treating other drugs of abuse, such as cocaine. Tiagabine is a drug that enhances levels of gamma aminobutyric acid (GABA), a chemical found in the brain and spinal cord. The objective of this study is to determine the effectiveness of tiagabine in modifying cocaine-using behavior and reducing opiate withdrawl symptoms among newly admitted methadone-treated patients.

This 16-week, double-blind, placebo-controlled clinical trial will involve 120 participants who are both cocaine- and opioid- dependent. Participants will be randomly assigned to receive either tiagabine (32 mg each day) or placebo, while concurrently receiving methadone treatment. Baseline cocaine use will be determined during the first two weeks of treatment. The study will include three overlapping phases. The first phase will include a one-week fixed methadone induction (Week 1), as well as flexible methadone stabilization (Weeks 2-13). Phase two will consist of a 12-week treatment period (Weeks 2-13). This will consist of tiagabine induction and stabilization. Phase three will include a 4-week taper, detoxification, or transfer peroid (Weeks 14-17). After completion of treatment, a 3-month follow-up visit will occur.
Eligibility
Ages Eligible for Study: 18 Years - 65 Years, Genders Eligible for Study: Both
Criteria

Inclusion Criteria:

  • Currently not enrolled in methadone-maintenance treatment
  • Demonstration of current opioid dependence as determined by the study physician, a self-reported history of opioid dependence for one year, and a positive urine test for opiates
  • Current cocaine abuser with self-reported use of cocaine at least 1 time each week within the month prior to study entry, positive urine screen for cocaine, and score greater than 3 on the Severity Dependence Scale
  • Women of childbearing age are eligible under the following conditions: negative pregnancy test at initial screening, adequate contraceptive use throughout the study, monthly pregnancy tests, and acknowledgement of fetal toxicity risks due to medication

Exclusion Criteria:

  • Current diagnosis of other drug or alcohol dependence (other than opiates, cocaine, or tobacco)
  • Serious medical illness (e.g., major heart, kidney, endocrine, or liver disease, or serious neurological disorders, including history of seizures)
  • Current diagnosis of a serious psychiatric illness or history of psychosis, schizophrenia, or bipolar type I disorder
  • Suicidal or homicidal thoughts
  • Currently taking psychotropic medications
  • Women who are pregnant, nursing, refuse to use a reliable form of contraception, or refuse monthly pregnancy testing
  • Greater than 3 times the normal level in liver screening function test (SGOT or SGPT)

Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00129298

Connecticut
VA Connecticut Healthcare System, West Haven, Connecticut, 06516, United States; Recruiting
Gerardo Gonzalez, M.D. 203-932-5711 Ext. 5453 gerardo.gonzalez-haddad@yale.edu

Study chairs or principal investigators

Gerardo Gonzalez, M.D., Principal Investigator, Yale University

More Information
Study ID Numbers: NIDA-17782-1; R01-17782-1
Last Updated: August 30, 2005
Record first received: August 4, 2005
ClinicalTrials.gov Identifier: NCT00129298
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-02

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