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A Diagnosis and Treatment Optimization Study of Depression Based on the Neurological Mechanism of Reward System

Primary Purpose

Diagnosis and Treatment of Depression

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Escitalopram
Duloxetine
Mirtazapine
Sponsored by
Peking University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diagnosis and Treatment of Depression

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • first-episode, drug naive melancholic depression; remitted depression; schizophrenia patients; first-degree relatives of depressed patients.

Exclusion Criteria:

  • major somatic diseases; DSM-IV axis I other mental illness; personality disorder, mental retardation; drug and / or alcohol dependence; serious suicidal tendencies or suicidal behavior; pregnant or lactating women; MRI contraindications.

Sites / Locations

  • Yun-Ai SURecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

escitalopram

duloxetine

mirtazapine

Arm Description

Eligible patients were assigned to escitalopram treatment based on investigators' clinical practice.

Eligible patients were assigned to duloxetine treatment based on investigators' clinical practice.

Eligible patients were assigned to mirtazapine treatment based on investigators' clinical practice.

Outcomes

Primary Outcome Measures

Hamilton Rating Scale for Depression
remission defined by Hamilton Rating Scale for Depression < 7

Secondary Outcome Measures

Full Information

First Posted
May 9, 2017
Last Updated
December 11, 2019
Sponsor
Peking University
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1. Study Identification

Unique Protocol Identification Number
NCT03148522
Brief Title
A Diagnosis and Treatment Optimization Study of Depression Based on the Neurological Mechanism of Reward System
Official Title
Clinical Psychopharmacology Division,Institute of Mental Health,Peking University
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
December 30, 2021 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Major depressive disorder (MDD) is a high-disabling disease. But its etiology and pathogenesis is not clear, and early recognition, diagnosis and treatment still has many challenges. Among numerous clinical manifestations of MDD, anhedonia is an important core symptom of MDD, especially in patients with melancholic features. Our previous studies and studies abroad have shown that MDD patients had functional abnormality in reward circuit. The abnormalities of reward-related core areas, such as the prefrontal cortex - nucleus accumbens - ventral tegmental area were closely associated with the development of MDD, and is an important neural basis of anhedonia. This study would take the reward circuit as mainline to carry out the etiology, diagnosis and therapeutic intervention studies of MDD. We would collect MDD patients with melancholic features and other populations with reward dysfunction. The neuroimaging techniques, stress assessment, genetic testing and drug intervention methods would be mainly used in this study. The functional connectivity of reward regions, such as the ventral striatum, nucleus accumben, and ventral medial prefrontal cortex, would be analyzed to identify the dysfunction of reward circuit of MDD, and its implication for early recognition, diagnosis and prediction of treatment efficacy of antidepressants. We would also investigate the effect of genetic and environmental factors on reward function of MDD and its biological basis. Finally, through modulating the reward circuit activity using animal experiments, we would verify and investigate reward dysfunction of MDD and its biological mechanisms. The project is expected to provide for new evidence for the establishment of reward mechanism - based objective diagnosis and treatment optimization strategy of MDD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diagnosis and Treatment of Depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
escitalopram
Arm Type
Experimental
Arm Description
Eligible patients were assigned to escitalopram treatment based on investigators' clinical practice.
Arm Title
duloxetine
Arm Type
Experimental
Arm Description
Eligible patients were assigned to duloxetine treatment based on investigators' clinical practice.
Arm Title
mirtazapine
Arm Type
Experimental
Arm Description
Eligible patients were assigned to mirtazapine treatment based on investigators' clinical practice.
Intervention Type
Drug
Intervention Name(s)
Escitalopram
Intervention Description
receive escitalopram
Intervention Type
Drug
Intervention Name(s)
Duloxetine
Intervention Description
receive duloxetine
Intervention Type
Drug
Intervention Name(s)
Mirtazapine
Intervention Description
receive mirtazapine
Primary Outcome Measure Information:
Title
Hamilton Rating Scale for Depression
Description
remission defined by Hamilton Rating Scale for Depression < 7
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: first-episode, drug naive melancholic depression; remitted depression; schizophrenia patients; first-degree relatives of depressed patients. Exclusion Criteria: major somatic diseases; DSM-IV axis I other mental illness; personality disorder, mental retardation; drug and / or alcohol dependence; serious suicidal tendencies or suicidal behavior; pregnant or lactating women; MRI contraindications.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ji-Tao Li, MD
Phone
010-62723742
Email
ljt_102124@163.com
Facility Information:
Facility Name
Yun-Ai SU
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100191
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yun-Ai Su, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35788366
Citation
Lin J, Su Y, Rizvi SJ, Jagoda J, Li J, Wu Y, Dai Y, Zhang Y, Kennedy SH, Si T. Define and characterize the anhedonia in major depressive disorder: An explorative study. J Affect Disord. 2022 Sep 15;313:235-242. doi: 10.1016/j.jad.2022.06.082. Epub 2022 Jul 3.
Results Reference
derived

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A Diagnosis and Treatment Optimization Study of Depression Based on the Neurological Mechanism of Reward System

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