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Clinical Trials/ITMCTR2200005972
ITMCTR2200005972
Not yet recruiting
Phase 1

Auricular electroacupuncture based on MRI brain imaging and intestinal flora in the treatment of depression and gut-brain axis mechanism and prediction of efficacy

Conditionsdepression

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
depression
Sponsor
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • (1\) Meet the ICD\-10 classification criteria for moderate\-to\-mild (2 core symptoms \+ 2 accompanying symptoms), moderate (2 core symptoms \+ 3\-4 accompanying symptoms) depression classification criteria; (2\) The disease duration ranges from 2 weeks to 7 points in 2 years \= HAMD\-17 score \= 24 points; (3\) The age is between 18 and 70 years old, and the gender is not limited; (4\) The education level is above junior high school, and can understand the content of the scale and cooperate with the research; (5\) Volunteered to participate in this study and signed the informed consent.

Exclusion Criteria

  • (1\) Patients with severe depression, or patients with severe mental illness, such as schizophrenia, mania, and those with obvious suicidal tendencies; (2\) Depressive disorders caused by psychoactive substances or non\-addictive substances; (3\) Patients with Patients with organic brain diseases; (4\) patients with serious physical diseases, such as heart disease, tumors or organic lesions of the central nervous system; (5\) patients with other neurological diseases, such as epilepsy, Parkinson's disease (6\) Pregnant or breastfeeding women; (7\) Those with low compliance or unable to adhere to treatment for other reasons; (8\) Those who are allergic to the study drug or have contraindications to fMRI scanning; (9\) Those who did not sign the informed consent form.

Outcomes

Primary Outcomes

Not specified

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