ClinicalTrials.Veeva

Menu

N-Acetyl Cysteine Plus Naltrexone in Methamphetamine Dependence

The University of Chicago logo

The University of Chicago

Status and phase

Completed
Phase 2

Conditions

Methamphetamine Dependence

Treatments

Drug: Placebo
Drug: Naltrexone plus N-Acetyl Cysteine

Study type

Interventional

Funder types

Other

Identifiers

NCT00332605
0601M80486

Details and patient eligibility

About

The goal of the proposed study is to evaluate the efficacy and safety of N-Acetyl Cysteine (NAC) in combination with naltrexone in methamphetamine dependence.

Full description

Forty subjects with DSM-IV methamphetamine dependence will receive 8 weeks of double-blind combination medication (NAC plus naltrexone) or placebo. The hypothesis to be tested is that NAC plus naltrexone will be effective and well tolerated in patients with methamphetamine dependence compared to placebo. The proposed study will provide needed data on the treatment of a public health crisis that currently lacks a clearly effective treatment.

Enrollment

45 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. men and women age 18-65
  2. current DSM-IV methamphetamine dependence.

Exclusion criteria

  1. unstable medical illness
  2. history of seizures
  3. myocardial infarction within 6 months
  4. current pregnancy or lactation, or inadequate contraception in women of childbearing potential
  5. any thoughts of suicide
  6. lifetime history of DSM-IV bipolar disorder type I, dementia, or schizophrenia or any other DSM-IV psychotic disorder
  7. previous treatment with N-Acetyl Cysteine or naltrexone
  8. treatment with investigational medication or depot neuroleptics within 3 months, with fluoxetine within 6 weeks, or with other psychotropics within 2 weeks prior to study baseline
  9. abnormal liver function tests at screening
  10. diagnosis of asthma
  11. current use of opiates.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 2 patient groups, including a placebo group

Naltrexone plus N-Acetyl Cysteine
Experimental group
Description:
Naltrexone tablets N-Acetyl Cysteine: 600mg tablets, daily
Treatment:
Drug: Naltrexone plus N-Acetyl Cysteine
Placebo
Placebo Comparator group
Description:
Inactive placebo ("sugar pill")
Treatment:
Drug: Placebo

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems