Study on the Gut Microbial Mechanism of Negative Symptoms of Schizophrenia
NCT ID: NCT04533724
Last Updated: 2020-09-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
EARLY_PHASE1
6 participants
INTERVENTIONAL
2020-10-01
2022-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Study group
Recruit 30 outpatient/inpatient schizophrenia patients (dominant negative symptoms) in Shanghai Mental Health Center .
Amisulpride
The amisulpride treatment group was given amisulpride tablets. The dose: the initial dose was 50 mg/d. The doctor titrated the dose to the therapeutic amount within 1 to 2 weeks according to the patient's condition. The maximum dose was 300 mg/d, taken with a single meal. Observe for 8 weeks.
Healthy control group
15 cases of normal healthy people (control group) with similar eating habits and ages in the same region were matched with study group.
No interventions assigned to this group
Interventions
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Amisulpride
The amisulpride treatment group was given amisulpride tablets. The dose: the initial dose was 50 mg/d. The doctor titrated the dose to the therapeutic amount within 1 to 2 weeks according to the patient's condition. The maximum dose was 300 mg/d, taken with a single meal. Observe for 8 weeks.
Eligibility Criteria
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Inclusion Criteria
* Meet the diagnostic criteria of "Schizophrenia" in the American Diagnostic Standards for Mental Disorders (DSM-V);
* The first attack, no antipsychotic drugs have been used in the past six months;
* The PANSS negative symptom subscale has at least 3 items with 4 points and above or at least two items with 5 points and above, and the positive symptoms score is less than 19 points;
* The negative symptom score is at least 6 points or more higher than the positive symptom score;
* The cultural, social and educational background is sufficient to understand informed consent and research content.
Exclusion Criteria
* .G6≥4 points in PANSS, or CDSS≥6 points;
* .SAS Side Reaction Scale\> 3 points;
* Organic diseases of the central nervous system;
* In the past two months, there were people who were dependent or abused on alcohol or other substances, which caused significant impairment of social and cognitive function;
* In the past year, there have been major life events such as widowhood;
* Serious suicide attempts;
* .The current patient's severe and unstable physical disease;
* .Pregnant and lactating women;
* Have a history of antibiotic use of more than 3 days within 3 months;
* Use probiotics (lactic acid products, etc.) for more than 3 days within 3 months;
* Type 1 diabetes and severe diabetes complications;
* .Digestive system diseases such as gastrointestinal inflammation, acute or chronic hepatitis;
* .Severe organ diseases, such as cancer, coronary heart disease, myocardial infarction, cerebral hemorrhage;
* .Have infectious diseases, such as tuberculosis, AIDS;
* Drug treatment of cholecystitis, peptic ulcer, urinary tract infection, acute nephritis, cystitis or hyperthyroidism.
18 Years
45 Years
ALL
Yes
Sponsors
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Shanghai Mental Health Center
OTHER
Responsible Party
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Principal Investigators
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Qinyu Lv
Role: PRINCIPAL_INVESTIGATOR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Qi Zhang
Role: STUDY_CHAIR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Zhenghui Yi
Role: STUDY_CHAIR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Congze Wang
Role: STUDY_CHAIR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Huanling Zhang
Role: STUDY_CHAIR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Xinxin Huang
Role: STUDY_CHAIR
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
Central Contacts
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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2020LQY
Identifier Type: -
Identifier Source: org_study_id
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