Dose Response of Mirtazapine to Methamphetamine Induced Interest, Mood Elevation and Reward

Withdrawn before enrolling · Not applicable · Has a placebo group

Conditions studied: Amphetamine Dependence

In brief

The primary purpose of this study is to determine if Mirtazapine will produce a decrease in interest in the drug, a decrease in mood elevation, and/or a decrease in reward when given before methamphetamine compared to placebo. Participants will be screened with a psychiatric interview, medical history and physical, laboratory tests, drug of abuse screen and, if female, a urine pregnancy test. They will be provided written informed consent. They will be studied in a within-subjects examination of the subjective mood responses of mirtazapine and methamphetamine. Interactions between methamphetamine and mirtazapine will be assessed by pharmacokinetic studies. Each participant will be introduced to rating scales and cognitive tasks described below. Participants will remain in the research unit for 5 hours on each day that they receive study medication or placebo. They will spend five days in total on the research unit, one day separated by at least one day; then in two day blocks separated by at least one day from another two day block. A venous catheter will be placed for blood draws. Blood pressures and heart rates will be recorded and assessed. Participants will be randomized and double blinded to receive either placebo or mirtazapine orally two hours prior to the administration of randomized and double blinded methamphetamine or placebo in order to have the peak effects of the drugs overlap. VAS-mood, ARCI, GRS, POMS and POMS-E, neurocognitive tasks Trails A and B and Symbol digits modalities test will be administered prior to the mirtazapine or placebo dose, and repeated after the administration of methamphetamine or placebo. After the administration of methamphetamine or placebo, vital signs will be assessed every 15 minutes and the measures will be repeated until 120 minutes have passed from the initial dose of methamphetamine or placebo. Blood will be drawn at one, three and four hour marks for pharmacokinetic testing. This will be repeated on each testing day.

Key facts

Study ID

NCT00600145

Run by

University of Virginia

People needed

0

Starts

2007-09-01

Expected to finish

2010-07-01

Last updated by the study team

2011-04-27

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 -45 years old
• healthy human volunteers
• no history of pre-existing physical (including cardiovascular) illness
• no history of drug abuse or dependence (defined below)
• ability to read and write

You may not qualify if…

• pregnant
• any psychotropic medication
• criteria for active substance abuse or dependence based on the DSM-IV: For substance abuse: A maladaptive pattern of substance use leading to clinically significant impairment or distress, as manifested by one (or more) of the following, occurring within a 12-month period:
• recurrent substance use resulting in a failure to fulfill major role obligations at work, school, home (e.g., repeated absences or poor work performance related to substance use; substance-related absences, suspensions, or expulsions from school; neglect of children or household)
• recurrent substance use in situations in which it is physically hazardous (e.g., driving an automobile or operating a machine when impaired by substance use)
• recurrent substance-related legal problems (e.g., arrests for substance-related disorderly conduct)
• continued substance use despite having persistent or recurrent social or interpersonal problems caused or exacerbated by the effects of the substance (e.g., arguments with spouse about consequences of intoxication, physical fights)
• The symptoms have never met the criteria for Substance Dependence for this class of substances.
• For substance dependence: A maladaptive pattern of substance use, leading to clinically significant impairment or distress, as manifested by three (or more) of the following, occurring at any time in the same 12-month period:
• tolerance, as defined by either of the following:
• a need for markedly increased amounts of the substance to achieve intoxication or desired effect
• markedly diminished effect with continued use of the same amount of substance
• withdrawal, as manifested by either of the following:
• the characteristic withdrawal syndrome for the substance
• the same (or a closely related) substance is taken to relieve or avoid withdrawal symptoms
• the substance is often taken in larger amounts or over a longer period than was intended
• there is a persistent desire or unsuccessful efforts to cut down or control substance use
• a great deal of time is spent in activities to obtain the substance, use the substance, or recover from its effects
• important social, occupational or recreational activities are given up or reduced because of substance use
• the substance use is continued despite knowledge of having a persistent or recurrent physical or psychological problem that is likely to have been caused or exacerbated by the substance (e.g., continued drinking despite recognition that an ulcer was made worse by alcohol consumption) on any stimulant medication including:
• Amphetamine (Adderall®, Adderall XR®)
• Dextroamphetamine (Dexedrine®)
• Methamphetamine (Desoxyn®)
• Dexmethylphenidate (Focalin®, Focalin® XR)
• Diethylpropion (Tenuate®, Tenuate Dospan®)

Where it is running

• Universiyt of Virginia — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.