Status:

UNKNOWN

Dextromethorphan, Memantine Monotherapy, or Combined Use of Dextromethorphan and Memantine in Amphetamine Addiction

Lead Sponsor:

National Cheng-Kung University Hospital

Collaborating Sponsors:

Ministry of Science and Technology, Taiwan

Conditions:

Amphetamine Addiction

Pharmacotherapy

Eligibility:

All Genders

20-65 years

Phase:

PHASE2

PHASE3

Brief Summary

The investigators will conducted a randomized double-blind placebo-controlled study to investigate the treatment outcomes of add-on low dose dextromethorphan (DM), memantine (MM), or dextromethorphan ...

Detailed Description

The investigators will conducted a randomized double-blind placebo-controlled study to investigate the treatment outcomes of add-on low dose dextromethorphan (60mg/day, DM), memantine (5 mg/day, MM), ...

Eligibility Criteria

Inclusion

  • Signed informed consent by patient or legal representative.
  • Male or female patient aged ≧20 and ≦65 years.
  • A diagnosis of ATSUD according to DSM criteria made by a specialist in psychiatry.
  • Patient or a reliable caregiver can be expected to ensure acceptable compliance and visit attendance for the duration of the study.

Exclusion

  • The presence of any of the following will exclude a patient from study enrollment:
  • Women of childbearing potential, not using adequate contraception as per investigator judgment or not willing to comply with contraception for the duration of the study.
  • Females who are pregnant or lactation.
  • Other major Axis-I DSM-IV diagnosis other than ATSUD, except for tobacco use disorder, ATS induced mood or psychotic disorders.
  • Current evidence of an uncontrolled and/or clinically significant medical condition, e.g., cardiac, hepatic and renal failure that would compromise patient safety or preclude study participation.
  • History of allergy or intolerable side effects of DM or MM.
  • Suicidal attempts or risks during screen or study period.
  • Presence of active infectious or autoimmune disease.

Key Trial Info

Start Date :

August 11 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

July 31 2024

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT04687566

Start Date

August 11 2020

End Date

July 31 2024

Last Update

December 29 2020

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Department of Psychiatry, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University

Tainan, Taiwan, 70428