Neuroimaging MAO-B in Medication Free TR-MDD Using Novel Tracer

NCT ID: NCT02153281

Last Updated: 2019-05-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

8 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2019-05-31

Brief Summary

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The purpose of this study is to determine if monoamine oxidase B (MAO-B) total distribution volume (VT), after phenelzine treatment and if so to what extent.

Detailed Description

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Subjects will receive a PET and MRI scan before and after treatment with phenelzine.

Conditions

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Major Depressive Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Phenelzine treatment

Subjects will undergo a PET and MRI scan before and after the treatment.

Group Type EXPERIMENTAL

phenelzine treatment

Intervention Type OTHER

Subjects will have a PET and MRI scan before and after treatment with phenelzine.

Interventions

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phenelzine treatment

Subjects will have a PET and MRI scan before and after treatment with phenelzine.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18-80 years of age
* good physical health
* Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) diagnosis of current major depressive episode (MDE)
* DSM-IV diagnosis of major depressive disorder (MDD) verified by SCID for DSM-IV and a psychiatric consultation
* greater than 17 on the 17 item HDRS (Hamilton Depression Rating Scale).
* history of non-response to several different antidepressant classes

Exclusion Criteria

* herbal, drug or medication use (that affect CNS function)
* suicide attempts
* drug or medication use within eight weeks (+5 half lives of medication)
* history of substance abuse or any neurotoxin use
* history of psychotic symptoms
* history of central nervous system (CNS) medical illness
* current substance abuse
* test positive on pregnancy test (for women)
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre for Addiction and Mental Health

OTHER

Sponsor Role lead

Responsible Party

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Jeff Meyer

Head Neurochemical Imaging in Mood Disorders

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jeffrey H. Meyer, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Research Imaging Centre, Centre for Addiction and Mental Health

Locations

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Center for Addiction and Mental Health

Toronto, Ontario, Canada

Site Status

Countries

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Canada

Related Links

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http://www.camh.ca/research

Information about research at the Centre for Addiction and Mental Health

Other Identifiers

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DETB-071-13

Identifier Type: -

Identifier Source: org_study_id

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