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Clinical Trials/NCT04518592
NCT04518592
Recruiting
Not Applicable

Model-based Defining of Subtypes of Depression and Optimal Treatment: an Integrated Techniques Module in Multidimensional Omics for Peripheral Biomarkers.

Shanghai Mental Health Center1 site in 1 country300 target enrollmentDecember 22, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Depressive Disorder
Sponsor
Shanghai Mental Health Center
Enrollment
300
Locations
1
Primary Endpoint
reductive scores of Montgomery-Asberg Depression Rating Scale(MADRS)
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

In this proposal, the investigators aim to explore the clinical subtypes and biological markers to personalize the use of antidepressants in MDD. By stratifying the subjects with (versus without) remission and treatment response, the biological markers are expected to have important prediction effects in future clinical practice.

Detailed Description

In this proposal, through the integration of genome, transcriptome, protein, metabolic group, microbial group and immune cell subtype of multidimensional omics data to construct the curative effect of forecast model.The investigators aim to explore the clinical subtypes and biological markers to personalize the use of antidepressants in MDD. By stratifying the subjects with (versus without) remission and treatment response, the biological markers are expected to have important prediction effects in future clinical practice.Ultimate aim is to solve the depression medication selection dilemma of "trial and error", reduce medical costs, improving depression treatment experience.

Registry
clinicaltrials.gov
Start Date
December 22, 2020
End Date
September 30, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female subjects aged 18-65 years, outpatients or inpatients.
  • Meets the DSM-V criteria for Severe Major Depressive Disorder ; a single episode(296.21、296.22、296.23)or recurrent episode (296.31、296.32、296.33);
  • MADRS score greater than or equal to 24 in baseline;
  • HAMD-17 score greater than or equal to 20 in baseline.
  • Patients have learned and voluntarily participated in the study, and have to sign informed consent.

Exclusion Criteria

  • Meets the DSM-V criteria for other mental disorder(schizophrenia spectrum and other psychotic disorders, bipolar and related disorders, anxiety disorders, obsessive-compulsive and related disorders, somatic symptom and related disorders, etc ).
  • Patient has survived suicide attempt , or may have a significant risk for suicidal behavior ,or with a score of \>3 on suicidal thoughts item 10 on the MADRS.
  • Depressive episode of an organic mental disorder secondary to a systemic disease or a central nervous system disease, such as depressive episode secondary to hypothyroidism.
  • Serious and instable body disease such as cerebrovascular disease, respiratory disease, blood disease, liver and kidney disease, disease of internal secretion, nervous system and other systemic disease.
  • any history of seizures or other organic brain diseases.
  • History of alcohol or drug abuse (besides nicotine) over the last 6 months
  • Serious and instable body disease such as cerebrovascular disease, liver and kidney disease, disease of internal secretion (abnormal thyroid function), blood disease; any history of seizures or other organic brain diseases.
  • Subjects who can't take drug or have an operation history which affect drug metabolism.
  • Clinically significant changes in ECG or laboratory tests, including \>1.5X upper limit of normal liver function、over the limit of normal renal function and blood sugar、abnormal cardiac troponins、obvious abnormity in the thyroid function
  • Pregnant or lactating women and women of childbearing potential throughout the study period; men who have the desire of fertility within three months;

Outcomes

Primary Outcomes

reductive scores of Montgomery-Asberg Depression Rating Scale(MADRS)

Time Frame: assess the scale at baseline and week 8.

change in MADRS scores from baseline and week 8

Secondary Outcomes

  • The Montreal Cognitive Assessment(assess the scale at baseline and week 4, 8.)
  • effective rate(assess the scale at baseline and week 8.)
  • Response rate(assess the scale at baseline and week 8.)
  • Hamilton Anxiety Scale(assess the scale at baseline and week 4, 8.)
  • The Pittsburgh Sleep Quality Index(assess the scale at baseline and week 4, 8.)
  • The Quick Inventory of Depressive Symptomatology (16-Item) (Self-Report)(assess the scale at baseline and week 4, 8.)
  • Montgomery-Asberg Depression Rating Scale(MADRS) scores(assess the scale at baseline and week 4, 8.)
  • Subtraction score(assess the scale at baseline and week 4, 8.)
  • The overall evaluation of illness(assess the scale at baseline and week 4, 8.)

Study Sites (1)

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