跳至主要内容
临床试验/NCT02994433
NCT02994433
终止
1 期

NMDA Receptor Antagonist Nitrous Oxide Targets Affective Brain Circuits

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 49 人2017年1月27日

概览

阶段
1 期
干预措施
Nitrous Oxide
疾病 / 适应症
Depressive Disorder, Major
发起方
Washington University School of Medicine
入组人数
49
试验地点
1
主要终点
Comparison of functional connectivity between dorsal nexus of treatment-resistant depressed and non-depressed participants
状态
终止
最后更新
4年前

概览

简要总结

Most clinical major depression responds to standard treatments (medication and psychotherapy); however, a significant subset of depressed patients (15-20%) do not respond to these treatments and are referred to as treatment-resistant major depression (TRMD). New treatments for TRMD are needed, and one promising line of research are drugs known as N-methyl-D-aspartate (NMDA) glutamate receptor antagonists. In a recent pilot study, our group demonstrated that the NMDA antagonist nitrous oxide is effective in TRMD. This application proposes to take the next important step in understanding how nitrous oxide exerts its effects in the human brain by using state-of-the-art brain neuroimaging (functional connectivity magnetic resonance imaging) in a group of non-depressed, healthy volunteers and comparing the results to a group of TRMD patients.

This study involves exposing 20 non-depressed healthy participants and 20 TRMD participants to nitrous oxide and a placebo gas, to compare their brain images before and after each of the inhalation sessions. Sessions will be separated by at least one month to prevent treatment effects from carrying over into the following session. All willing and eligible subjects will undergo up to six functional connectivity MRI scans, and two inhalation sessions. Functional imaging in the brain will allow us to trace the interconnections between various parts of the brain, including those involved with emotion and depression.

Other procedures will involve screening materials to ensure safety of the participants before beginning the study (i.e. no MRI scan contraindications) and that subjects meet eligibility criteria to being in the targeted age range, depression/non-depressed state, neurological disorder history, and no medication exclusions.

注册库
clinicaltrials.gov
开始日期
2017年1月27日
结束日期
2020年2月28日
最后更新
4年前
研究类型
Interventional
研究设计
Crossover
性别
All

研究者

入排标准

入选标准

  • Adults 18-65 years of age
  • Right-handed
  • Controls: Not meet The Fourth Edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) criteria for major depressive disorder (MDD) by scoring ≤7 on the Hamilton Depression Rating Scale (HDRS), 17-item; Treatment-Resistant Major Depression (TRMD) patients: Must meet a ≥17 score on the HDRS.
  • Controls: Must not have any history of depression as determined by reported history and medical record review; TRMD: Documented (chart review) failure to respond to ≥3-4 adequate dose/duration antidepressant treatments; ≥1 in the current depressive episode.
  • Good command of the English language

排除标准

  • Meets criteria for any DSM-IV Axis I diagnosis as documented in medical records and as determined by structured clinical interview (except MDD for the TRMD group)
  • Known primary neurological disorders or medical disorders including dementia, stroke, encephalopathy Parkinson's Disease, brain tumors, multiple sclerosis, seizure disorder, severe cardiac or pulmonary disease
  • Any central nervous system active medication as determined by study investigator
  • Any known disease affecting drug metabolism and excretion (e.g. renal or liver disease) as determined by study investigator
  • Left-handedness
  • Not eligible for MRI scans (e.g. history of claustrophobia/implanted metal as per MRI Screening Tool)
  • Current use of psychotropic medications, antidepressants, or prescription or non-prescription drugs/herbals intended to treat depression or anxiety (control group only)
  • Any recent (within past 12 months) history of substance dependence or abuse, determined by reported history or urine drug screen
  • Ability to become pregnant and not using effective contraception
  • Contraindication against the use of nitrous oxide:

研究组 & 干预措施

Nitrous Oxide

One hour inhalation of nitrous oxide

干预措施: Nitrous Oxide

Nitrous Oxide

One hour inhalation of nitrous oxide

干预措施: MRI

Placebo Gas

One hour inhalation of placebo gas

干预措施: Placebo gas

Placebo Gas

One hour inhalation of placebo gas

干预措施: MRI

结局指标

主要结局

Comparison of functional connectivity between dorsal nexus of treatment-resistant depressed and non-depressed participants

时间窗: 2 hours after inhalation

Functional connectivity is measured between groups after inhaling nitrous oxide/placebo using an individual seed-voxel z map and pared t-test group analysis to identify effects on inter-regional connectivity.

Comparison of functional connectivity between default mode network of treatment-resistant depressed and non-depressed participants

时间窗: 2 hours after inhalation

Functional connectivity is measured between groups after inhaling nitrous oxide/placebo using an individual seed-voxel z map and pared t-test group analysis to identify effects on inter-regional connectivity.

Comparison of functional connectivity between affective network of treatment-resistant depressed and non-depressed participants

时间窗: 2 hours after inhalation

Functional connectivity is measured between groups after inhaling nitrous oxide/placebo using an individual seed-voxel z map and pared t-test group analysis to identify effects on inter-regional connectivity.

Comparison of functional connectivity between cognitive control network of treatment-resistant depressed and non-depressed participants

时间窗: 2 hours after inhalation

Functional connectivity is measured between groups after inhaling nitrous oxide/placebo using an individual seed-voxel z map and pared t-test group analysis to identify effects on inter-regional connectivity.

研究点 (1)

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