Sign in
Taking people in United StatesPhase 2

Mirtazapine for the Treatment of Methamphetamine Use in Opioid Use Disorder Patients Receiving Medication Assisted Treatment

Key facts

Who runs it
Washington State University
Where
Spokane, United StatesSee the site
Trial code
Status
Recruiting
Phase
Phase 2
People taking part
60 people, planned
Started
17 Jun 2024
Expected to end
1 Dec 2026
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • Mirtazapine
  • Placebo
Record updated
2 July 2026

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 25 criteriaShow less

Who can take part

  • Enrollment at medication for opioid use disorder (MOUD) treatment at Oregon Recovery \& Treatment Center/clinics in Spokane, WA
  • Verification of a DSM-5104 diagnosis of an methamphetamine (MA) use disorder (i.e. mild, moderate, or severe),
  • Aged 18+ years,
  • Ability to provide written informed consent,
  • Demonstration of 78% adherence rate during the induction period and
  • Provision of at least one MA positive urinalysis at baseline or during induction
  • Baseline complete blood cell count (CBC), total protein, albumin, glucose, alkaline phosphatase, creatinine, BUN, and electrolytes without clinically significant abnormalities as determined by clinician in conjunction with symptoms, physical exam, and medical history
  • No current acute illness requiring prolonged medical care
  • No serious chronic illnesses that are likely to progress clinically during trial participation
  • Vital signs are within the normal ranges (i.e., Blood pressure: 90/60 mm Hg to 120/80 mm Hg; breathing: 12-18 breaths per minute; pulse: 60-100 beats per minute; temperature: 97.8 - 99.1 degrees Fahrenheit

Who cannot take part

  • Prior diagnosis of dementia,
  • Currently taking 1) any type of opioid use disorder medication other than methadone or buprenorphine/naloxone, or 2) phenytoin, carbamazepine, or another inducer of hepatic metabolism (such as rifampicin) and CYP enzyme inhibitor cimetidine
  • Taking an anti-depressant medication within the past 30 days, including mirtazapine or a monoamine oxidase inhibitor,
  • Inability to demonstrate competency to provide informed consent because of cognitive or psychiatric disorders or limited English proficiency,
  • Current severe cocaine, amphetamine, or alcohol use disorder as defined by DSM-5 criteria which Drs Layton and McPherson deem their participation as unsafe
  • History of bipolar disorder or psychotic disorder, as determined by Structured Clinical Interview for DSM Disorders (SCID,
  • History of violent criminal behavior or being on parole,
  • Moderate or severe liver disease (AST, ALT, and total bilirubin >= 5 times upper limit of normal),
  • Impaired renal function (estimated GFR <40 ml/min),
  • Medically or psychiatrically unsafe to participate as determined by Dr. Layton (Medical Director),
  • Documented suicide attempt in the past 30 days and/or serious suicide intention or plan as assessed by the Structured Clinical Interview for DSM-5 (SCID-5; clinical trials version)105
  • Suicide attempt in the last 2 years
  • Prescribed MZP in the least year, or
  • Currently pregnant or intending to become pregnant,
  • Final determination of eligibility will be made by Dr. Layton in consultation with the PI

Where in United States

  • Spokane Treatment CenterSpokane, United StatesContact: Rachel Ryan, BSTaking people

About the trial

What the trial wants to find out

This project will evaluate the ability of Mirtazapine (MZP), a pharmacologically unique medication with a growing body of evidence to support its efficacy and safety for the treatment of methamphetamine (MA) use among medication for opioid use disorder (MOUD) patients, to significantly decrease MA use and related health-impairing behaviors. MZP has already successfully been used in the treatment of methamphetamine (detailed further below and in the Appendices).

Read full original descriptionShow less

The investigators hypothesize that those assigned to the MZP plus treatment as usual (TAU) MZP+TAU arm will demonstrate significantly increased rates of biochemically verified abstinence from MA and other substances of abuse and experience improvements in health impairing behaviors relative to the placebo (PLO)+TAU arm across the 10-week treatment and follow-up periods.

The 2 groups in the trial

  • MZP+TAUTreatment being tested

    Mirtazapine + Treatment as Usual

    Treatment: Mirtazapine

  • PLO+TAUPlacebo, for comparison

    Placebo + Treatment as Usual

    Treatment: Placebo

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
A Phase II Randomized, Double-blind, Placebo-controlled Clinical Trial (RCT) to Evaluate the Ability of Mirtazapine (MZP) to Increase Methamphetamine (MA) Abstinence Among Treatment-seeking Medication for Opioid Use Disorder (MOUD) Adults
Record updated
2 July 2026