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Clinical Trials/JPRN-UMIN000049967
JPRN-UMIN000049967
Recruiting
未知

Multi-institutional clinical study of patients with major depressive disorder and healthy participants to examine the usefulness of the brain network marker program using fMRI for the diagnosis and stratification of major depressive disorder - Multi-institutional clinical study to examine the usefulness of the brain network marker program using fMRI for the diagnosis of major depressive disorder

Tokyo Medical and Dental University0 sites520 target enrollmentMarch 24, 2023

Overview

Phase
未知
Intervention
Not specified
Conditions
Patients with major depressive disorder and healthy participants
Sponsor
Tokyo Medical and Dental University
Enrollment
520
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 24, 2023
End Date
September 30, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • \[Patients] (1\)Patients with mental status that makes it difficult to understand the purpose of the study. (2\)Patients who meet any of the following criteria: \-Patients with depression with psychotic features. \-Patients who have been diagnosed with bipolar disorder or schizophrenia using DSM. \-Patients who have been diagnosed with substance abuse within 6 months prior to obtaining consent. \-Patients who have been treated for an anxiety disorder within 6 months prior to obtaining consent. \-Patient who have a comorbid personality disorder at the time of consent acquisition. (3\)Patients with significant suicidal tendencies. (4\)Patients with contraindications to MRI. (5\)Patients who are deemed inappropriate as research participants by the principal investigator or a subinvestigator. \[Healthy participants] (1\)Participants with current or history of psychiatric or neurological disorders. (2\)Participants with contraindications to MRI. (3\)Participants who are deemed inappropriate as research participants by the principal investigator or a subinvestigator.

Outcomes

Primary Outcomes

Not specified

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