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Résztvevőt keres itt: Egyesült Államok2. fázis

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

A legfontosabb adatok

Ki végzi
Washington State University
Hol
Spokane (Egyesült Államok)A helyszín megnézése
Azonosító
Állapot
Toboroz
Fázis
2. fázis
Résztvevők
60 fő, tervezett
Kezdés
2024. jún. 17.
Várható befejezés
2026. dec. 1.
A vizsgálat típusa
Beavatkozással járó, 2 csoportAz egyik csoport placebót (hatóanyag nélküli szert) kap, összehasonlításként.
A vizsgált kezelések
  • Mirtazapine
  • Placebo
A regiszteradat frissítve
2026. július 2.

Ki vehet részt

Életkor
18 év felett
Nem
Nők és férfiak
Egészséges önkéntesek
Részt vehetnek

A regiszter feltételei, szó szerint

Mind a 25 feltétel megnézéseKevesebb

Ki vehet részt

  • 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

Ki nem vehet részt

  • 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

Helyszínek itt: Egyesült Államok

  • Spokane Treatment CenterSpokane, Egyesült ÁllamokContact: Rachel Ryan, BSRésztvevőt keres

A vizsgálatról

Mit akar kideríteni a vizsgálat

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).

A teljes eredeti leírásKevesebb

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.

A vizsgálat 2 csoportja

  • MZP+TAUA vizsgált kezelés

    Mirtazapine + Treatment as Usual

    Kezelés: Mirtazapine

  • PLO+TAUPlacebo, összehasonlításként

    Placebo + Treatment as Usual

    Kezelés: Placebo

Kérdések a vizsgálat csapatának

  1. Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
  2. Megtérítik az utazási költséget?
  3. Megtarthatom a saját orvosomat?
  4. Mi történik, ha ki akarok lépni?

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

Oldal nyomtatása az orvosomnak

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
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
A regiszteradat frissítve
2026. július 2.
Építés alatt, nem éles – Mirtazapine for the Treatment of Methamphetamine Use in Opioid Use Disorder Patients Receiving Medication Assisted Treatment (NCT06323837) – Frontlight Research