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Clinical study of Kaixin Changyu granule in the treatment of post-stroke depressio

Phase 1
Recruiting
Conditions
Post stroke depression
Registration Number
ITMCTR2100004842
Lead Sponsor
The First Affiliated Hospital of Dalian Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Refer to the Key Points for Diagnosis of Various Cerebrovascular Diseases revised by the Chinese Medical Association to be diagnosed with stroke;
2. According to the Chinese Classification and Diagnosis of Mental Disorders-Third Edition (CCMD-III), subjects diagnosed with secondary mild to moderate depression, Hamilton Depression Scale (HAMD-17) 17 items Score between 7 and 24 points;
3. The age of the subject is between 40 and 80 years old, regardless of gender;
4. Patients who were diagnosed with depression for the first time after stroke (diagnosed as PSD within 6 months after stroke);
5. No history of mental illness or family history of mental illness before stroke;
6. Normal consciousness can cooperate with various examinations, no aphasia or severe cognitive impairment, mental status examination (MMSE score)> 17 points;
7. Liver and kidney function tests are normal;
8. Be able to provide a voluntary signed informed consent form.

Exclusion Criteria

1. Participate in any other clinical trials or take hormones and psychotropic drugs within the last 1 month;
2. Unstable vital signs, poor control of underlying diseases, or serious systemic diseases such as heart disease or malignant tumors;
3. Allergic to the ingredients of Kaixin Changyu Granules;
4. Pregnant or lactating women;
5. Magnetic resonance contraindications.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Homocysteine;High sensitivity C-reactive protein;Related scales;FA value of DTI;
Secondary Outcome Measures
NameTimeMethod
Incidence of adverse reactions;
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