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临床试验/NCT04005053
NCT04005053已完成2 期

Identifying Biological Signatures of N-Acetylcysteine for Non-Suicidal Self-Injury in Adolescents and Young Adults

University of Minnesota1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2019年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
44
试验地点
1
主要终点
Percent Increase in Glutathione (GSH) Concentrations in the ACC

研究概览

简要总结

To measure NAC-induced changes to concentrations of glutathione (GSH) in the anterior cingulate cortex (ACC) as measured by magnetic resonance spectroscopy (MRS) in 36 adolescents and young adults with NSSI (12 in each group: high, low, and placebo).

详细描述

This study is a double-blind, placebo controlled, 4-week course of two-tiered N-acetylcysteine (NAC) dosing focused on identifying the optimal dose to achieve meaningful change in measurable biomarkers (glutathione and glutamate).

This design will allow us to confirm acute biological changes, select the optimal dose for achieving biological effects, and examine dose/concentration-response relationships with respect to biological markers and pharmacokinetics.

Brief schedule of activities: Subjects will be recruited through community and clinical settings and screened over the phone. There will be a total of 4 in-person visits and two sets of on-line study activities.

Eligible participants will be assigned to one of 3 groups (double-blinded): a low-dose NAC group (3600 mg/day), a high-dose NAC group (5400mg/day), and placebo (PBO). The study intervention period is 4 weeks. Total participation is up to 8 weeks, depending on the length of time between Day 0 and Day 1.

The investigators will recruit 36 adolescents and young adults aged 16-24 years. There will be 12 participants in each group (PBO, 3600mg/day, 5400mg/day). The investigators will use a minimization procedure to ensure that the participants in these 3 groups will have similar age, clinical severity and medication status.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
16 Years 至 24 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Current frequency of at least one NSSI episode in the past 2 months
  • ≥ 5 past episodes of NSSI with significant tissue damage (e.g. scars present)
  • Psychotropic medications are dose-stable for 1 month
  • Ability to understand study procedures and to comply with them for the entire length of the study

排除标准

  • Any MRI contraindications (e.g. metal plates, claustrophobia, braces, implanted devices)
  • Any current serious medical illness as defined by medical history
  • Current Substance Use Disorder (except Tobacco Use Disorder)
  • Primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder, schizophreniform disorder)
  • Neurodevelopmental disorder such as mental retardation or autism
  • Changes in psychotropic medications in past 1 month
  • Taken NAC or glutathione on a regular basis in the past 6 months
  • Currently pregnant, planning to become pregnant, currently breastfeeding, or unwillingness to use contraception throughout the study.
  • Allergy/sensitivity to N-acetylcysteine.
  • Inability or unwillingness of individual or legal guardian/representative to give written informed consent.

研究组 & 干预措施

Low-Dose NAC

Experimental

3600 NAC mg/day

干预措施: N-acetyl cysteine (Drug)

High-Dose NAC

Experimental

5400 NAC mg/day

干预措施: N-acetyl cysteine (Drug)

Placebo

Placebo Comparator

Placebo

干预措施: Placebo oral tablet (Drug)

结局指标

主要结局

Percent Increase in Glutathione (GSH) Concentrations in the ACC

时间窗: 28 days

increase in glutathione (GSH) concentrations in the anterior cingulate cortex (ACC) as measured by magnetic resonance spectroscopy (MRS)

次要结局

  • Change in GSH Reduced-to-oxidized Ratio(28 days)
  • Change in Glutamate Concentrations(28 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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