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Amantadine in methamphetamine-dependent patients

The assessment of amantadine add-on therapy effects on craving and relapse reduction among patients with methamphetamine dependence.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090801002266N16
Enrollment
64
Registered
2022-02-09
Start date
2022-03-01
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Craving and relapse reduction in methamphetamine-dependent patients.

Interventions

Intervention 1: Intervention group: The intervention group will be treated with a daily dose of 100 mg amantadine capsules (Hakim, Iran) that will be increased by 100 mg every week to achieve the maxi
if tolerated by the patients. The matrix program will be performed for two months with the latest dose and by the end of the program, the medication will be ce

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 18-60 years old patients The participants who meet the criteria of methamphetamine use disorder based on DSM-V Only depend on methamphetamine Patients' satisfaction for participation in the study

Exclusion criteria

Exclusion criteria: Psychiatric drugs administration The concurrent major psychiatric disorders such as mood and thinking disorders Major and chronic physical disorders Pregnancy

Design outcomes

Primary

MeasureTime frame
The amantadine add-on therapy effects on craving and relapse reduction among patients with methamphetamine dependence. Timepoint: Methamphetamine urine test will be done weekly during the intervention and monthly in follow-up period. Method of measurement: CCQ-Brief Questionnaire.

Secondary

MeasureTime frame
Anxiety. Timepoint: Before and 2 months after the Intervention. Method of measurement: Hospital Anxiety - Depressive Scale.;Depression. Timepoint: Before and 2 months after the Intervention. Method of measurement: Hospital Anxiety - Depressive Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholam Reza Kheirabadi

Esfahan University of Medical Sciences

kheirabadi@bsrc.mui.ac.ir+98 31 1222 2135

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026