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Neurochemical, Metabonomics and Neuroimaging Characterization of TCM Diagnostic Subtypes of Major Depression Disorder (NMNTDM)

Primary Purpose

Severe Major Depression Disorder

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
venlafaxine
Sponsored by
Zhejiang Provincial Tongde Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Severe Major Depression Disorder focused on measuring major depression disorder, biochemistry, TCM diagnosis, Neurological, metabonomics, neuroimaging

Eligibility Criteria

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

Inclusion Criteria:

  1. Had a diagnosis of major depressive disorder according to DSM-V and TCM criteria of 'pattern of Liver Depression and Qi Stagnation (LDQS)' or'pattern of Deficiency of Both Heart and Spleen (DBHS)
  2. The severity of the symptoms is moderate or severe, confirmed by a 35 or greater of Hamilton Rating Scale for Depression(HAMD) score
  3. Absence of brain and/or severe physical diseases
  4. 18-65years old

Exclusion Criteria:

  1. In pregnancy,brain and other severe medical conditions
  2. Psychoactive substance abuse
  3. Had a diagnosis of bipolar disorder

Sites / Locations

  • Tongde hospital of zhejiang provinceRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

LDQS group

DBHS group

the normal controls group

Arm Description

Liver Depression and Qi Stagnation (LDQS)group,Liver Depression and Qi Stagnation Syndrome should include at least the following 5 symptoms and signs: emotional depression or sadness, pessimism, short breath, sigh, dysphoria,thin coating,stringy pulse Drugs use generic name :Venlafaxine; Dosage form:capsule Dosage, frequency and duration:Venlafaxine dose was initiated at 75 mg/day and escalated to an optimal dose (150-225 mg/day in most cases) within 2 week, depending upon individual patient response, but the maximum dose could not exceed 300 mg/day during the next 4 weeks. The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline and after 6-week venlafaxine administration.

Deficiency of Both Heart and Spleen (DBHS) group,Deficiency of Both Heart and Spleen Syndrome should include at least following 6 symptoms and signs: emotional depression, thinking torpidity, tiredness, forgetfulness, insomnia, loose stool, sweating, pale tongue body, thin tongue coating, and thin and deep pulse Drugs use generic name :Venlafaxine; Dosage form:capsule Dosage, frequency and duration:Venlafaxine dose was initiated at 75 mg/day and escalated to an optimal dose (150-225 mg/day in most cases) within 2 week, depending upon individual patient response, but the maximum dose could not exceed 300 mg/day during the next 4 weeks. The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline and after 6-week .

The normal controls group including the healthy volunteer None drug The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline .

Outcomes

Primary Outcome Measures

Brain neuroimaging
Diffusion Tensor Imaging(DTI) is used to detect changes in FA maps of brain white matter fiber in major depressive patients

Secondary Outcome Measures

Biochemical tests
Gas Chromatography-Mass Spectrum is used to test blood and urine samples for: lactic acid, alanine, 3 - hydroxy butyric acid, valine, carbamide, glycerinum, phosphoric acid, isoleucine, glycine, succinic acid, threonine, malic acid, glutamic acid, citric acid, stearic acid, GABA, methionine, cysteine, lysine, tryptophan, leucine, methionine and tyrosine.

Full Information

First Posted
December 18, 2014
Last Updated
April 23, 2015
Sponsor
Zhejiang Provincial Tongde Hospital
Collaborators
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT02346682
Brief Title
Neurochemical, Metabonomics and Neuroimaging Characterization of TCM Diagnostic Subtypes of Major Depression Disorder
Acronym
NMNTDM
Official Title
Neurochemical,Metabonomics and Neuroimaging Characterization of TCM Diagnostic Subtypes of Major Depression Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhejiang Provincial Tongde Hospital
Collaborators
The University of Hong Kong

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is heterogeneity in patients with depression. Many scholars propose that individualization of antidepressant achieves better outcomes. However, the scientific theoretical basis of individualized treatment is still quite weak. Different clinical subtypes of depression and their possible biomarkers are critically needed to provide the individualization with theoretical base. Diagnostic types of major depression disorder (MDD) based on the Theory of Traditional Chinese Medicine (TCM) and possible differentiations in neurobiochemistry, metabonomics and neuroimaging could be one of ways to explore the biomarkers and support the theory of the individualized treatment. The hypothesized results will be of help to clarify the biological basis of MDD with LDQS and with DBHS, to provide the TCM with further scientific evidence, to explore the pathogenesis of depression, to improve the objective diagnosis of depression, and to promote targeted interventions by Western medicine, TCM or both.
Detailed Description
The objectives of this study is to explore if there are any differences in neurobiochemistry, metabonomics and neuroimaging (1) at the baseline, between the subjects who are the normal controls (C Group) and who both meet diagnostic criteria of the Diagnostic and Statistical Manual of 5th edition (DSM-V) on MDD and TCM criteria of 'pattern of Liver Depression and Qi Stagnation (LDQS)' or'pattern of Deficiency of Both Heart and Spleen (DBHS)' (T Group); (2) at the baseline, between the MDD subjects of LDQS and DBHS; (3) after 6-week venlafaxine administration, between the MDD subjects of LDQS and DBHS. 50 subjects in T Group and 25 in C Group are recruited in the study and the main laboratory tests include High Performance Liquid Chromatography(HPLC), Gas Chromatography-Mass Spectrum(GCMS) and neuroimaging DTI technology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Major Depression Disorder
Keywords
major depression disorder, biochemistry, TCM diagnosis, Neurological, metabonomics, neuroimaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
75 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LDQS group
Arm Type
Active Comparator
Arm Description
Liver Depression and Qi Stagnation (LDQS)group,Liver Depression and Qi Stagnation Syndrome should include at least the following 5 symptoms and signs: emotional depression or sadness, pessimism, short breath, sigh, dysphoria,thin coating,stringy pulse Drugs use generic name :Venlafaxine; Dosage form:capsule Dosage, frequency and duration:Venlafaxine dose was initiated at 75 mg/day and escalated to an optimal dose (150-225 mg/day in most cases) within 2 week, depending upon individual patient response, but the maximum dose could not exceed 300 mg/day during the next 4 weeks. The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline and after 6-week venlafaxine administration.
Arm Title
DBHS group
Arm Type
Active Comparator
Arm Description
Deficiency of Both Heart and Spleen (DBHS) group,Deficiency of Both Heart and Spleen Syndrome should include at least following 6 symptoms and signs: emotional depression, thinking torpidity, tiredness, forgetfulness, insomnia, loose stool, sweating, pale tongue body, thin tongue coating, and thin and deep pulse Drugs use generic name :Venlafaxine; Dosage form:capsule Dosage, frequency and duration:Venlafaxine dose was initiated at 75 mg/day and escalated to an optimal dose (150-225 mg/day in most cases) within 2 week, depending upon individual patient response, but the maximum dose could not exceed 300 mg/day during the next 4 weeks. The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline and after 6-week .
Arm Title
the normal controls group
Arm Type
No Intervention
Arm Description
The normal controls group including the healthy volunteer None drug The biomarkers of neurobiochemistry, metabonomics and neuroimaging would be tested at the baseline .
Intervention Type
Drug
Intervention Name(s)
venlafaxine
Other Intervention Name(s)
clonazepam
Intervention Description
Venlafaxine dose was initiated at 75 mg/day and escalated to an optimal dose (150-225 mg/day in most cases) within 2 week, depending upon individual patient response, but the maximum dose could not exceed 300 mg/day during the next 4 weeks. Patients were prescribed a combination of venlafaxine and Benzodiazepines for sleep disturbance.
Primary Outcome Measure Information:
Title
Brain neuroimaging
Description
Diffusion Tensor Imaging(DTI) is used to detect changes in FA maps of brain white matter fiber in major depressive patients
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Biochemical tests
Description
Gas Chromatography-Mass Spectrum is used to test blood and urine samples for: lactic acid, alanine, 3 - hydroxy butyric acid, valine, carbamide, glycerinum, phosphoric acid, isoleucine, glycine, succinic acid, threonine, malic acid, glutamic acid, citric acid, stearic acid, GABA, methionine, cysteine, lysine, tryptophan, leucine, methionine and tyrosine.
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Neurochemical tests
Description
High Performance Liquid Chromatography (HPLC) is used to detect blood samples for: 5-HT, NE, DA, 5-HTAA, and HVA.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Had a diagnosis of major depressive disorder according to DSM-V and TCM criteria of 'pattern of Liver Depression and Qi Stagnation (LDQS)' or'pattern of Deficiency of Both Heart and Spleen (DBHS) The severity of the symptoms is moderate or severe, confirmed by a 35 or greater of Hamilton Rating Scale for Depression(HAMD) score Absence of brain and/or severe physical diseases 18-65years old Exclusion Criteria: In pregnancy,brain and other severe medical conditions Psychoactive substance abuse Had a diagnosis of bipolar disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lan-ying Liu, Master
Organizational Affiliation
Zhejiang Provincial Tongde Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Tongde hospital of zhejiang province
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310012
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Feng Bin, bachelor
Phone
+860571 89972003
Email
fengbintd@aliyun.com
First Name & Middle Initial & Last Name & Degree
Zhang jianmin, Ph.d
Phone
+86057189972008
Email
jianmin.3.zhang@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Zhang-jin Zhang, Professor
First Name & Middle Initial & Last Name & Degree
Bin Feng, Professor
First Name & Middle Initial & Last Name & Degree
Jiong Chen, physician
First Name & Middle Initial & Last Name & Degree
ya-ping Li, Professor
First Name & Middle Initial & Last Name & Degree
Jin-bao Pu, researcher
First Name & Middle Initial & Last Name & Degree
Wei-qing Liang, researcher
First Name & Middle Initial & Last Name & Degree
Hong-xia Zhang, Radiologist
First Name & Middle Initial & Last Name & Degree
Wen-song Chen, physician
First Name & Middle Initial & Last Name & Degree
Zheng-xin Chen, physician
First Name & Middle Initial & Last Name & Degree
Cheng-yu Gu, physician
First Name & Middle Initial & Last Name & Degree
Pei-rong Wang, physician
First Name & Middle Initial & Last Name & Degree
Yong-chun Ma, physician
First Name & Middle Initial & Last Name & Degree
Yin Zhang, physician
First Name & Middle Initial & Last Name & Degree
Chun-yu Yang, physician
First Name & Middle Initial & Last Name & Degree
Bao-ping Xing, physician
First Name & Middle Initial & Last Name & Degree
Wei-dong Jin, physician
First Name & Middle Initial & Last Name & Degree
Yuan-Yuan Zhang, physician

12. IPD Sharing Statement

Citations:
PubMed Identifier
31044001
Citation
Liu LY, Xu XP, Luo LY, Zhu CQ, Li YP, Wang PR, Zhang YY, Yang CY, Hou HT, Cao YL, Wang G, Hui ES, Zhang ZJ. Brain connectomic associations with traditional Chinese medicine diagnostic classification of major depressive disorder: a diffusion tensor imaging study. Chin Med. 2019 Apr 11;14:15. doi: 10.1186/s13020-019-0239-8. eCollection 2019.
Results Reference
derived
PubMed Identifier
30386416
Citation
Liu LY, Zhang HJ, Luo LY, Pu JB, Liang WQ, Zhu CQ, Li YP, Wang PR, Zhang YY, Yang CY, Zhang ZJ. Blood and urinary metabolomic evidence validating traditional Chinese medicine diagnostic classification of major depressive disorder. Chin Med. 2018 Oct 25;13:53. doi: 10.1186/s13020-018-0211-z. eCollection 2018.
Results Reference
derived

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Neurochemical, Metabonomics and Neuroimaging Characterization of TCM Diagnostic Subtypes of Major Depression Disorder

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