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NCT06746831
Methamphetamine Isomer Pharmacology in Humans
Conditions: Methamphetamine
Sex: All
Ages: 21 Years – 64 Years
Healthy volunteers: Yes
Phase: PHASE1
Enrollment: 17
Sponsor: University of Wisconsin, Madison
Location: University of Wisconsin Madison Wisconsin
Summary
This study is being done to understand the metabolism and impairment profile of methamphetamine (meth). Meth exists as two chemical structures that are mirror images of each other: R-meth and S-meth. S-meth is a strong central nervous system stimulant and used to treat attention deficit disorder (ADD). R-meth is not a strong central nervous system stimulant and is available over-the-counter in nasal decongestant sprays.17 healthy participants will be enrolled for 3 study visits and on study for up to 12 weeks.
Eligibility Criteria
Inclusion Criteria:
* Good mental health as determined by self-reported responses to the Psychopathology Screener
* Absence of any major cardiac, neurologic, psychiatric, oncologic, endocrine, metabolic, renal, or hepatic disease as determined by self-reported responses to the Medical History Screener
* English-speaking (able to provide consent and complete questionnaires)
* Written Informed Consent
Exclusion Criteria:
* Any serious prior adverse response to sympathomimetic agents or amphetamine analogs
* History of or current substance use disorder as determined by self-reported responses to the Internalizing, Externalizing, and Substance Use Disorder Screener
* Pregnancy or lactation (pregnancy test, if needed)
* Use of medications that may impact cognition or metabolism (e.g., mood stabilizers, sedatives)
* Dependent on prohibited concomitant therapy that cannot be withheld for 48 hours prior to and during study visits.
Source: ClinicalTrials.gov (NCT06746831). StuddyBuddy aggregates publicly available trial information.