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Clinical Trials/KCT0004102
KCT0004102
Recruiting
未知

Efficacy of Clinical Application of Transcranial Low Intensity Focused Ultrasound Stimulation for Patients with Major Depressive Disorder - Exploratory Clinical Trial

Yonsei University Health System, Gangnam Severance Hospital0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Yonsei University Health System, Gangnam Severance Hospital
Enrollment
60
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Yonsei University Health System, Gangnam Severance Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\) Montgomery\-Asberg Depression Rating Scale (MADRS) score of 12 or more
  • 2\) Patients who did not start medication or who maintained a MADRS score of 20 points or more for antidepressant treatment for 4 weeks or more

Exclusion Criteria

  • 1\) Patients who can not undergo Brain CT and MRI
  • 2\) Brain CT showed a skull thickness of more than 8 mm or a clinically significant calcification
  • 3\) Patients with structural abnormalities such as brain tumors, cerebral hemorrhage, traumatic brain disease, or changes due to degenerative brain disease in MRI
  • 4\) Patients with physical illnesses that may cause depressive symptoms (thyroid dysfunction, uncontrolled diabetes, etc.) or those taking medication that may cause depressive symptoms
  • 5\) Patients with a history of epileptic seizures
  • 6\) Patients with coexisting major psychiatric disorders such as schoziphrenia or bipolar disorder (identified as MINI)
  • 7\) Patients suspected of having intellectual disability (discriminated by short\-form intelligence test)
  • 8\) Patients with severe physical illness (cancer, tuberculosis, etc.)
  • 9\) Persons with sensitive skin disease including contact skin dermatitis
  • 10\) Pregnant women or women planning pregnancy

Outcomes

Primary Outcomes

Not specified

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