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Chinese Longitudinal and Systematic Study of Bioplar Disorder (CLASS-BD)

Primary Purpose

Major Depressive Disorder, Bipolar Disorder, Mixed, Affective; Disorder, Organic

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Escitalopram Oxalate Tablets
Quetiapine Fumarate Tablets
Lurasidone
Sponsored by
First Affiliated Hospital of Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring Major Depressive Disorder, Bipolar Disorder, Affective Disorder, Gut-Brain Axis

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Both biological parents are Han nationality;
  2. Aged 16-65;
  3. The subjects met the clinical diagnostic criteria of DSM-5 for depressive episodes of MDD/BD;
  4. Did not take any immunomodulatory preparations within 1 month before enrollment;
  5. No clear history of respiratory tract, urinary system, digestive system infection within 1 month before enrollment;

Exclusion Criteria:

  1. Those with schizophrenia spectrum, neurodevelopmental disorder, dementia, memory impairment or other cognitive impairment that meet the DIAGNOSTIC criteria of DSM-5;
  2. Mental disorders caused by substance abuse (alcohol, drugs, etc.), patients suffering from serious physical diseases and immune system diseases, such as diabetes, thyroid diseases, hypertension, heart disease, liver and kidney dysfunction, autoimmune diseases, etc.;
  3. Had received medication (such as antidepressants, antipsychotics, mood stabilizers, etc.) within 1 month before enrollment;
  4. those who had used ECT before enrollment;
  5. Currently have serious suicidal thoughts or behaviors, or serious excitement;
  6. those who cannot follow the doctor's advice or have no guardian;
  7. pregnant or breast-feeding women, or those who plan to become pregnant;
  8. Contraindications to MRI examination;
  9. Other conditions that the researcher considers inappropriate for inclusion.

Sites / Locations

  • The First Affiliated Hospital of Zhejiang UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

bipolar disorder

major depressive disorder

healthy control

Arm Description

Patients with BD depressive episode received standard treatment with quetiapine fumarate tablets, starting from 50mg/ night, titrated to a therapeutic dose of 300-400mg/ night within 10 days, and maintained treatment for 4 weeks. According to the patient's condition, patients with BD depressive episode could receive another standard treatment with lurasidone, starting from 20mg/ night, titrated to a therapeutic dose of 40mg/ night within 6 days, and maintained treatment for 4 weeks. Adverse reactions and changes in condition of all patients were recorded

MDD depressive episode patients received standard treatment with escitalopram oxalate tablets, starting from 5mg/ day once, titrated to a therapeutic dose of 10-20mg/ day within 1 week, and maintained treatment for 4 weeks

no interventions

Outcomes

Primary Outcome Measures

Montgomery-Asberg Depression Rating Scale(MADRS)
MADRS score is to evaluate the degree of depression, and the higher score means severer depression.

Secondary Outcome Measures

Full Information

First Posted
July 28, 2022
Last Updated
October 13, 2022
Sponsor
First Affiliated Hospital of Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT05480150
Brief Title
Chinese Longitudinal and Systematic Study of Bioplar Disorder
Acronym
CLASS-BD
Official Title
Chinese Longitudinal and Systematic Study of Bioplar Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First Affiliated Hospital of Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Affective disorders (mainly including major depressive disorder and bipolar disorder) are common, chronic and highly disabling mental disorders, which lack of objective biological markers. It is believed that genetic and environmental factors are involved in the development of affective disorders. Gut microbes can affect the function of brain neural circuits by mediating metabolic, immune, endocrine and autonomic changes along the brain-gut axis. The brain can also regulate intestinal microbes through endocrine, neural structure, neurogenic exosomes and other pathways. Based on the brain-gut axis, this study intends to establish a large cohort of affective disorders, and screen out efficient and convenient biomarkers for clinical diagnosis and efficacy prediction by studying key indicators such as intestinal microbes, serum metabolites and immune indexes, brain-derived exosomes, and brain functional imaging.
Detailed Description
Mental health is a major public health problem affecting the whole social and economic development. According to a 2019 report in The Lancet Psychiatry, the weighted lifetime prevalence of mental disorders (excluding dementia) in China is 16.6%, with the lifetime prevalence of emotional disorders as high as 7.4%.Affective disorders (mainly including depression and bipolar disorder) are common, chronic and highly disabling mental disorders.Back in 2008, the World Health Organization listed MDD(Major Depressive Disorder) as one of the three major contributors to the overall global burden of disease. It is expected that by 2030, the number of MDD patients will exceed the total number of cardiovascular disease patients combined and become the leading cause of disability in the world. At present, the diagnostic criteria of mental disorders, including DSM-5 and ICD-11, still mainly rely on the evaluation of symptoms, lacking objective and intuitive biomarkers. Therefore psychiatrists are prone to disagreement in diagnosis and treatment of diseases, which is a realistic bottleneck hindering the development of psychiatry. The differential diagnosis of MDD and BD depressive episodes is an unavoidable clinical challenge, which often leads to misdiagnosis and affects the treatment and prognosis of the disease. Therefore, it is one of the important directions for the development of brain science to strengthen scientific research in the field of mental health, especially to explore the mechanism of disease occurrence and development, develop objective new auxiliary diagnostic technologies and innovate precise treatment strategies around major emotional disorders. It is believed that genetic and environmental factors are involved in the development of affective disorders. Gut microbes can affect the function of brain neural circuits by mediating metabolic, immune, endocrine and autonomic changes along the brain-gut axis. The brain can also regulate intestinal microbes through endocrine, neural structure, neurogenic exosomes and other pathways. This study based on brain - im axis, intends to create an emotional disorder large queue, through the study of gut microbes (diversity and abundance of species), serum metabolites, and immune index, brain outside source sex secretion, brain imaging and other key indicators, select high efficiency and convenient for clinical diagnosis and curative effect of prediction of biomarkers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Bipolar Disorder, Mixed, Affective; Disorder, Organic
Keywords
Major Depressive Disorder, Bipolar Disorder, Affective Disorder, Gut-Brain Axis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
bipolar disorder
Arm Type
Experimental
Arm Description
Patients with BD depressive episode received standard treatment with quetiapine fumarate tablets, starting from 50mg/ night, titrated to a therapeutic dose of 300-400mg/ night within 10 days, and maintained treatment for 4 weeks. According to the patient's condition, patients with BD depressive episode could receive another standard treatment with lurasidone, starting from 20mg/ night, titrated to a therapeutic dose of 40mg/ night within 6 days, and maintained treatment for 4 weeks. Adverse reactions and changes in condition of all patients were recorded
Arm Title
major depressive disorder
Arm Type
Experimental
Arm Description
MDD depressive episode patients received standard treatment with escitalopram oxalate tablets, starting from 5mg/ day once, titrated to a therapeutic dose of 10-20mg/ day within 1 week, and maintained treatment for 4 weeks
Arm Title
healthy control
Arm Type
No Intervention
Arm Description
no interventions
Intervention Type
Drug
Intervention Name(s)
Escitalopram Oxalate Tablets
Other Intervention Name(s)
Lexapro
Intervention Description
Starting at 5mg qn, the treatment dose was titrated to 10-20mg qn within 1 week and maintained for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Quetiapine Fumarate Tablets
Other Intervention Name(s)
Seroquel
Intervention Description
Starting at 50mg qn, the treatment dose was titrated to 300-400mg qn within 10 days, and maintained the treatment for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
Lurasidone
Other Intervention Name(s)
Latuda
Intervention Description
Starting at 20mg qn, the treatment dose was titrated to 40mg qn within 6 days,and maintained the treatment for 4 weeks.
Primary Outcome Measure Information:
Title
Montgomery-Asberg Depression Rating Scale(MADRS)
Description
MADRS score is to evaluate the degree of depression, and the higher score means severer depression.
Time Frame
0 ~16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Both biological parents are Han nationality; Aged 16-65; The subjects met the clinical diagnostic criteria of DSM-5 for depressive episodes of MDD/BD; Did not take any immunomodulatory preparations within 1 month before enrollment; No clear history of respiratory tract, urinary system, digestive system infection within 1 month before enrollment; Exclusion Criteria: Those with schizophrenia spectrum, neurodevelopmental disorder, dementia, memory impairment or other cognitive impairment that meet the DIAGNOSTIC criteria of DSM-5; Mental disorders caused by substance abuse (alcohol, drugs, etc.), patients suffering from serious physical diseases and immune system diseases, such as diabetes, thyroid diseases, hypertension, heart disease, liver and kidney dysfunction, autoimmune diseases, etc.; Had received medication (such as antidepressants, antipsychotics, mood stabilizers, etc.) within 1 month before enrollment; those who had used ECT before enrollment; Currently have serious suicidal thoughts or behaviors, or serious excitement; those who cannot follow the doctor's advice or have no guardian; pregnant or breast-feeding women, or those who plan to become pregnant; Contraindications to MRI examination; Other conditions that the researcher considers inappropriate for inclusion.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shaohua Hu
Phone
086-13957162903
Email
dorhushaohua@zju.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Yanmeng Pan
Phone
18868116237
Email
12018602@zju.edu.cn
Facility Information:
Facility Name
The First Affiliated Hospital of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hu ShaoHua
Phone
13957162903
Email
dorhushaohua@zju.edu.cn

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Arms and interventions can be shared, while the clinical data will not be shared

Learn more about this trial

Chinese Longitudinal and Systematic Study of Bioplar Disorder

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