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临床试验/NCT06835582
NCT06835582Enrolling By Invitation不适用

Assessing Concentrations of Methadone and Its Metabolites

Cari Health Inc.1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年3月17日最近更新:
相关药物

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
20
试验地点
1
主要终点
Measurement of whole blood methadone levels with Lateral Flow Assay

研究概览

简要总结

An observational proof of concept method comparison study. Comparing Liquid Chromatography -Mass Spectroscopy to a new Quantitative Lateral Flow Immunoassay with an Optical Reader.

详细描述

CARI Health, Inc.'s long-term goal is to address the problem of high dropout rates of patients receiving medication for opioid use disorder (MOUD; e.g., methadone) treatments, which has increased with the prevalence of fentanyl use, with an innovative point-of-care (PoC) device to enable science-based personalized dosing for patients receiving methadone treatment for opioid use disorder (OUD). The proposed solution consists of a customized analysis device that incorporates proprietary methadone detection technology for quickly measuring methadone and metabolite levels in the blood and calculating the methadone/metabolite ratio (MMR).

To accomplish this long-term goal, the investigators aim to first quantitatively measure methadone doses taken and ethylidene-dimethyl-diphenyl pyrrolidine (EDDP) detection using lateral flow assays. At this stage, the investigators are not testing a device. They are first assessing whether methadone metabolism can be evaluated using lateral flow assays, which are simple paper-based diagnostic strips. The tests work similarly to a home pregnancy test, where a sample (like blood, urine, or saliva) flows along a test strip and interacts with antibodies or other molecules that capture the target substance. No clinical decisions will be made, no treatment will be applied, and no dosing will be changed based on the results learned in this study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A prescription for methadone at a dose of 10mg or more for at least 7 days. Participants may be taking the methadone to treat an OUD or for pain. Taking methadone as prescribed during the last 4 days before consent to participate in the study.
  • Has been prescribed at least 1 day of take-home doses.
  • Exclusion criteria for methadone group includes:
  • Age <18 or >
  • A condition preventing or complicating blood collection. Conditions may include dermatological (skin) condition, bleeding diathesis, immunodeficiency, recent blood donation, anemia, end stage renal disease, liver cirrhosis, cancer, congestive heart failure, bleeding diathesis, tuberculosis (TB), active severe depression (e.g., suicidal ideation), or mania symptoms.
  • Tattoo or piercing close to sampling area. Under a conservatorship.

排除标准

  • 未提供

结局指标

主要结局

Measurement of whole blood methadone levels with Lateral Flow Assay

时间窗: 1 day

whole blood measurement of methadone

Measurement of whole blood methadone metabolite Levels with Lateral Flow Assay

时间窗: 1 day

Whole blood measurement of methadone metabolite

Measurement of plasma methadone with LC-MS

时间窗: 1 day

plasma methadone with LC-MS

Measurement of plasma methadone metabolite with LC-MS

时间窗: 1 day

plasma methadone metabolite with LC-MS

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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