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Effectiveness of NAC (N-Acetylcysteine) in the treatment of methamphetamine use disorder

Effectiveness of NAC (N-Acetylcysteine) in the treatment of methamphetamine use disorder: a randomized, double-blind, placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260423069144N1
Enrollment
42
Registered
2026-05-01
Start date
2026-07-06
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Methamphetamine use disorder.

Interventions

Intervention 1: Intervention group:The intervention group will receive 1200 mg NAC daily in two divided doses for 12 weeks, and the placebo group will receive a placebo similar in size and shape in th

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18 to 65 years Diagnosis of methamphetamine use disorder (MUD), based on DSM-5-TR Absence of acute or chronic physical disorders such as acute infection, cardiovascular, hepatic, or renal diseases in the past three months Absence of psychiatric disorders or history of suicide at least one month prior to study entry and no use of antidepressant medications in the past month (substance-induced psychotic and mood disorders are excluded) No current dependence on cocaine, alcohol, or benzodiazepines and no dependence on alcohol during the three years prior to study initiation Completion of the informed consent form for entry into the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in the substance craving score based on the Substance Craving Assessment Questionnaire. Timepoint: The substance craving test will be performed at baseline (before the start of the intervention) and at 4, 8, and 12 weeks after the start of the intervention. Method of measurement: Substance Craving Assessment Questionnaire.

Secondary

MeasureTime frame
Number of urine samples negative for methamphetamine and reduction in substance use based on urine test results. Timepoint: Before the start of the intervention and at weeks 4, 8, and 12 after the start of the intervention. Method of measurement: Urine sample.;Number of weeks of complete abstinence and treatment success rate. Timepoint: At baseline and at weeks 4, 8, and 12. Method of measurement: Treatment success will be defined as abstinence from methamphetamine for 21 days or self-reported reduction of methamphetamine use by more than 50% compared with baseline use.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShokouh Gheibi

University of social welfare and rehabilitation sciences

sho.gheibi@uswr.ac.ir+98 21 2214 2530

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026