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Clinical Trials/NCT00033072
NCT00033072
Unknown
Phase 1

Assessment of Potential Interactions Between Intravenous Methamphetamine and Oral Selegiline

National Institute on Drug Abuse (NIDA)1 site in 1 country16 target enrollmentSeptember 2001

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Amphetamine-Related Disorders
Sponsor
National Institute on Drug Abuse (NIDA)
Enrollment
16
Locations
1
Primary Endpoint
pharmacokinetic assessment
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to assess the potential interactions between intravenous methamphetamine and oral selegiline.

Detailed Description

To determine the safety of the selegiline concurrent with d-methamphetamine challenges of 15mg \& 30mg i.v. with the focus being on cardiovascular responses (HR,BP) to the i.v. methamphetamine challenges. This is a randomized, single-blind, placebo-controlled, two-arm study design to evaluate the safety of selegiline treatment, compared to placebo treatment, concurrent with i.v. methamphetamine challenges.

Registry
clinicaltrials.gov
Start Date
September 2001
End Date
October 2002
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Volunteers who meet DSM-4 criteria for methamphetamine abuse or dependence; non-treatment seeking individuals
  • Be able to verbalize understanding of consent form; provide written informed consent

Exclusion Criteria

  • Please contact site for more information

Outcomes

Primary Outcomes

pharmacokinetic assessment

safety of selegiline

Study Sites (1)

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