Spokane Treatment Center
Spokane, Washington, 99208, United States
Location status: Recruiting
Location contact
Rachel Ryan, BS
CONTACT
NCT Number: NCT06323837
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).
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Spokane, Washington, 99208, United States
Location status: Recruiting
Rachel Ryan, BS
CONTACT
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This is a Phase 2, 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.
Placebo to match.
Time frame: Weeks 2 to Week 22
Determine if participants randomized to the MZP+TAU arm use less MA compared to those assigned to the PLO+TAU arm. We hypothesize that those assigned to the MZP+TAU arm will demonstrate significantly increased rates of biochemically verified MA abstinence relative to those in the PLO+TAU arm across the 10-week treatment period and 3-month follow-up periods.
Time frame: Week 2 to Week 22
Determine if participants randomized to the MZP+TAU arm demonstrate improvements in sleep compared to those assigned to the PLO+TAU arm. We hypothesize that those assigned to the MZP+TAU arm will demonstrate improvements in objectively verified sleep relative to the PLO+TAU arm across the 10-week treatment and 3-month follow-up periods.
Time frame: Week 2 to Week 22
Determine if participants randomized to the MZP+TAU arm experience the same number of adverse events compared to those in the PLO+TAU arm. We hypothesize that those assigned to the MZP+TAU arm will demonstrate statistically equivalent numbers of adverse events relative to those in the PLO+TAU arm across the 10-week treatment and 3-month follow-up periods.
Time frame: Week 2 to Week 22
Determine if participants randomized to the MZP+TAU arm abstain from other substances of abuse (e.g. illicit opioids, cocaine) and demonstrate improvements in MA-associated health-impairing outcomes (e.g. cravings, sleep quality and HIV risk behavior) compared to those assigned to the PLO+TAU arm.
Contact information is provided by the study sponsor or research team.
Washington State University
Other
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
Acronym: MIRROM
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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