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临床试验/NCT04841798
NCT04841798已完成不适用

Monoamine Oxidase B Occupancy in Depressed Patients

Centre for Addiction and Mental Health2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
MAO-B occupancy of tranylcypromine at standard treating dose

研究概览

简要总结

The study is looking at assessing monoamine oxidase B (MAO-B) occupancy in depressed patients before and after medication treatment using positron emission tomography (PET) scan.

详细描述

BACKGROUND

1.1 Problem of Treatment Resistant Depression and a Proposed Solution

Problem of Major Depressive Disorder: Major depressive disorder (MDD) known to the layperson as clinical depression, is an illness composed of repeated major depressive episodes of variable length and persistence (MDE).

MDD is the leading cause of death and disability in moderate to high income countries. MDD is common with 5% of adults in the midst of a major depressive episode (MDE) and the lifetime prevalence of MDD is 10 to 20%. MDD is also often treatment resistant, with 50% of people having inadequate responses. Plausible Mechanism of Treatment Resistance: It is generally believed that there are multiple underlying pathologies in MDD and the mismatch of treatment to pathology results in treatment resistance. Hence it is important to determine whether common brain pathologies are targeted by common treatments like serotonin and norepinephrine reuptake inhibitors, and to establish the degree to which alternative treatments might better target such brain pathologies. Then with this information matching of treatment to identified disease pathologies can be optimized.

STUDY OBJECTIVES

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 18 to 80
  • DSM-5 diagnosis of current MDE and MDD verified by the research version of SCID for DSM-5
  • early onset type MDD with first MDE prior to age 40
  • score greater than or equal to 17 on the 17 item Hamilton Depression Rating Scale (HDRS)28
  • antidepressant free for at least 2 weeks (by self report)
  • worsening of MDE symptoms or new onset MDE symptoms after COVID-19 may receive rasagiline and complete all procedures except the second [11-C]SL25.1188 PET scan - participants with this criteria will be enrolled in the alternative criteria that is similar to the general criteria except for the second PET scan.

排除标准

  • history of psychotic symptoms
  • history of antisocial or borderline personality disorders (screened with the Structured Clinical Interview for Personality Disorders (SCID) for Diagnostic and Statistical Manual-5 (DSM-5) (unless occuring after COVID)
  • history of neurodegenerative illness
  • cigarette smoking for the past 6 months (there are reports that cigarette smoking lowers monoamine oxidase B 31, 32.)
  • currently abusing street drugs
  • current alcohol use disorder
  • diagnosis of liver or kidney disease
  • positive for hepatic dysfunction as measured by aspartate transaminase (AST) and alanine transaminase (ALT) tests
  • diagnosis of cardiovascular disease such as hypertension/hypotension, angina or tachycardia
  • electroconvulsive therapy or mechanical brain stimulation treatment within the previous 6 months (the effects of these on MAO-B level are unknown but since they could stimulate astrogliosis which could influence MAO-B level these are included as exclusionary)
  • positive pregnancy test (in our Centre women up to 65 years of age are given a urine pregnancy test prior to every PET scan)
  • currently breastfeeding
  • recent use of MAO-B inhibitor treatments (within the previous 4 weeks)
  • disorders of coagulation, blood or ongoing use of anticoagulant medication
  • presence of metal objects or implanted electrical devices in the body that would preclude MRI scanning
  • claustrophobia
  • weight over 400lbs and height over 7ft (requirements for fitting in the scanners and hospital gowns)
  • the total radiation dose over the currently approved guideline of 20 millisievert (mSv) in a 12-month period. Note: The sievert is a derived unit of ionizing radiation dose in the International System of Units (SI) and is a measure of the health effect of low levels of ionizing radiation on the human body.
  • history of undergoing a number of PET scans that, including the number of PET scans under this protocol, will bring the total to more than 8 PET scans/lifetime, exceeding permissible limit for subjects participating in research set by our centre's guidelines
  • elevated liver transaminases AST and ALT levels as shown by the laboratory test results
  • Additional Requirements for Receiving Tranylcypromine :
  • not taking any anesthetics, meperidine (Demerol), anti-asthmatics, anti-hypertensives, dextromethorphan, buspirone, narcotics, codeine (e.g. found in Tylenol), over the counter medication for colds, hay fever, sinus decongestants, eye drops that contain tetrahydrozoline hydrochloride (Visine); SSRI medication including selective reuptake inhibitors (SSRI), amitriptyline, nortriptyline, protriptyline, desipramine, imipramine, doxepin, perphenazine, carbamazepine, cyclobenzaprine, amoxapine, maprotiline, trimipramine; stimulant medication such as: amphetamines, ephedrine, cocaine, methylphenidate, methyldopa, dopamine, levodopa, tryptophan as well as energy-enhancing and weight-reducing preparations for at least 2 weeks
  • not taking fluoxetine for at least 6 weeks
  • inadequate response to serotonin reuptake inhibitor medication
  • inadequate response to medication that raises norepinephrine
  • inadequate response to lithium addition to an antidepressant or patient does not want to take lithium due to side effects (such as intention tremor or hypothyroidism risk)
  • inadequate response to a medication that raises both serotonin and norepinephrine
  • inadequate response to wellbutrin or participant is not able to take wellbutrin due to a contraindication or side effect or participant does not wish to take wellbutrin
  • inadequate response to wellbutrin added to a second antidepressant or participant is not able to take wellbutrin due to a contraindication or side effect or participant does not wish to take wellbutrin
  • awareness and willingness to follow medication and substance use requirements required of taking tranylcypromine or rasagiline
  • previous hypersensitivity to monoamine oxidase inhibitors
  • previous history of hypersensitivity to tyramine
  • self report of previous diagnosis of cerebrovascular or cardiovascular disorders
  • self report history of recurrent or frequent headaches
  • diagnosis of phaeochromocytoma and catecholamine-releasing paragangliomas
  • systolic blood pressure not between 91 and 139 mmHg (inclusive)
  • diastolic blood pressure not between 51 and 90 mmHg (inclusive)
  • a decrease in systolic blood pressure of 20 mm Hg or diastolic blood pressure of 10 mm Hg within three minutes of standing when compared with BP from the sitting position
  • use of triptans or tryptamines (e.g. sumatriptan or rizatriptan) in the past 2 weeks.
  • Additional Requirements for Taking Rasagiline
  • ● Participant does not wish to take tranylcypromine due to concerns regarding side effects or the strict dietary restrictions of reduced tyramine intake required for taking tranylcypromine.
  • Additional Requirements for Taking Duloxetine:
  • Participants must be antidepressant free for at least 4 weeks prior to scanning (most antidepressants affect monoamines as does duloxetine so a longer period of being medication free is required to be able to separate effect of duloxetine from previous medication).
  • Participant must not have a history of non-response to duloxetine at a daily dose of 60mg daily or higher.

结局指标

主要结局

MAO-B occupancy of tranylcypromine at standard treating dose

时间窗: 3 years

MAO-B Occupancy is an overall occupancy measure that is intended to be derived from Lassen Plot. The Lassen Plot will include MAO-B total distribution volume (VT) values before and after treatment in regions that optimize the plot. It is expected that these will include prefrontal cortex, anterior cingulate cortex, dorsal putamen, ventral striatum, hippocampus, and cerebellum. To quantify the regional monoamine oxidase B (MAO-B) occupancy we use a measure called the total distribution volume (VT) an index of MAO-B density. The percent change, termed occupancy can range from 0% to 100%.

MAO-B occupancy of rasagiline at standard treating dose

时间窗: 3 years

MAO-B Occupancy is an overall occupancy measure that is intended to be derived from Lassen Plot. The Lassen Plot will include MAO-B total distribution volume (VT) values before and after treatment in regions that optimize the plot. It is expected that these will include prefrontal cortex, anterior cingulate cortex, dorsal putamen, ventral striatum, hippocampus, and cerebellum. To quantify the regional monoamine oxidase B (MAO-B) occupancy we use a measure called the total distribution volume (VT) an index of MAO-B density. The percent change, termed occupancy can range from 0% to 100%.

次要结局

  • Rasagiline effect on MAO-B distribution volume (VT) in the prefrontal cortex(3 years)
  • Rasagiline effect on MAO-B distribution volume (VT) and cognition in MDE post COVID-19(3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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MAO-B Occupancy in Depressed Patients | 临床试验