Skip to content

Integration of Host Metabolome and Gut Microbiome for Predicting the Therapeutic Efficacy of Schizophrenia Drugs

Integration of Host Metabolome and Gut Microbiome for Predicting the Therapeutic Efficacy of Schizophrenia Drugs

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123010
Enrollment
Unknown
Registered
2026-04-21
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Interventions

First-episode drug-naive schizophrenia patients (patient group):None
Healthy controls:None

Sponsors

The Second People's Hospital of Yibin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for the patient group: (1) Diagnosis meets the DSM-5 criteria for schizophrenia. Patients are first-episode and have taken any psychiatric medication for no more than 3 days; (2) Aged between 16 and 55 years; (3) Han ethnicity; (4) Primary residence in the Chengdu area for the past 6 months; (5) Voluntary participation in this study with signed written informed consent. 2. Inclusion criteria for the healthy control group: (1) Resided in Southwest China for the past 6 months; (2) Aged between 16 and 55 years; (3) Han ethnicity; (4) No history of major surgery within the past 3 years; (5) Intact social functioning and full capacity for civil conduct.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for the patient group: (1) History or current presence of other mental disorders besides schizophrenia (such as intellectual disability, bipolar disorder, depression, etc.); (2) History or current presence of definite organic brain diseases; (3) Currently suffering from somatic diseases receiving any oral medication, or chronic diseases requiring long-term medication, such as diabetes, systemic lupus erythematosus, and hypertension; (4) Infectious digestive system diseases (such as bacterial enteritis, dysentery, intestinal tuberculosis, etc.) within the past 1 month; (5) Use of antibiotics, probiotics, prebiotics, etc. within the past 1 month; (6) Women in pregnancy or perinatal period within the past 1 year; (7) Unable to cooperate with testing, refusing to participate in this study, or withdrawing informed consent. 2. Exclusion criteria for the healthy control group: (1) History or current presence of any mental disorder; (2) History or current presence of definite organic brain diseases; (3) Currently suffering from somatic diseases receiving any oral medication, or chronic diseases requiring long-term medication, such as diabetes, systemic lupus erythematosus, and hypertension; (4) Infectious digestive system diseases (such as bacterial enteritis, dysentery, intestinal tuberculosis, etc.) within the past 1 month; (5) Use of antibiotics, probiotics, prebiotics, etc. within the past 1 month; (6) Unable to cooperate with testing, refusing to participate in this study, or withdrawing informed consent.

Design outcomes

Primary

MeasureTime frame
Positive and Negative Syndrome Scale (PANSS) Score;Relative Abundance of Dominant Gut Microbiota;Relative Concentration of Small Molecule Metabolites;Concentration of Short-Chain Fatty Acids;Dietary Pattern;Food Craving Intensity;Routine Inflammatory Markers (White Blood Cell Count, C-Reactive Protein, Interleukins, etc.);

Countries

China

Contacts

Public ContactWang Li

The Second People's Hospital of Yibin

596701143@qq.com+86 831 3580373

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026