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

P

Peking University

Status

Unknown

Conditions

Diagnosis and Treatment of Depression

Treatments

Drug: Escitalopram
Drug: Mirtazapine
Drug: Duloxetine

Study type

Interventional

Funder types

Other

Identifiers

NCT03148522
81630031

Details and patient eligibility

About

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.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts 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.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 3 patient groups

escitalopram
Experimental group
Description:
Eligible patients were assigned to escitalopram treatment based on investigators' clinical practice.
Treatment:
Drug: Escitalopram
duloxetine
Experimental group
Description:
Eligible patients were assigned to duloxetine treatment based on investigators' clinical practice.
Treatment:
Drug: Duloxetine
mirtazapine
Experimental group
Description:
Eligible patients were assigned to mirtazapine treatment based on investigators' clinical practice.
Treatment:
Drug: Mirtazapine

Trial contacts and locations

1

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Central trial contact

Ji-Tao Li, MD

Data sourced from clinicaltrials.gov

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