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Clinical Trials/NCT00442923
NCT00442923
Withdrawn
Phase 2

Scientific Component IV: Pharmacotherapy to Prevent Methamphetamine Relapse

Aaron J. Janowsky1 site in 1 countryJuly 1, 2007

Overview

Phase
Phase 2
Intervention
Coreg
Conditions
Anxiety
Sponsor
Aaron J. Janowsky
Locations
1
Status
Withdrawn
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this research study is to determine whether Carvedilol, an FDA approved beta blocker, when administered for an 8-week period to veterans currently undergoing treatment for methamphetamine dependence (1) improves their ability to stay in treatment longer, (2)eases the aversive symptoms that accompany stimulant withdrawal, and (3) increases the time they remain abstinent from methamphetamine.

Registry
clinicaltrials.gov
Start Date
July 1, 2007
End Date
June 30, 2011
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Aaron J. Janowsky
Responsible Party
Sponsor Investigator
Principal Investigator

Aaron J. Janowsky

Director, Methamphetamine Abuse Research Center

Oregon Health and Science University

Eligibility Criteria

Inclusion Criteria

  • Must have entered treatment into the outpatient Clinical Addiction Rehabilitation Section (CARS) through the US Portland Veterans Affairs Medical Center
  • Must meet the clinical definition for methamphetamine dependence
  • Self-reported methamphetamine use within 10 days of entering the study
  • Must be able to understand and sign the consent form

Exclusion Criteria

  • Dependent on any other drug except nicotine, caffeine, marijuana and alcohol
  • Pregnant or nursing mothers
  • Psychosis
  • Any serious medical condition that could be aggravated by the study protocol (Allergic reaction, Hypotension, Asthma, Bronchospastic conditions, Angina, Bronchitis, Emphysema, Bradycardia, Heart or blood vessel disease, Diabetes mellitus, Low blood sugar, Kidney disease, Liver disease or Overactive thyroid)
  • History of withdrawal seizures or delirium tremors
  • Use of MAO inhibitors within the last two weeks
  • Considerable hepatocellular injury, including cirrhosis of the liver or liver function test levels higher than 2 times normal

Arms & Interventions

CTRL

Intervention: Coreg

TREAT

Intervention: Coreg

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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