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Clinical Trials in China / NCT07162467
Enrolling by invitation Observational

Tryptophan-Kynurenine Pathway Metabolism in the Pathophysiology of Cognitive Impairment in Schizophrenia.

NCT07162467 · tracked via the Priya Life Science China tracker
Sponsor
Tianjin Anding Hospital
Phase
Observational
Started
2024-02-19
Last updated
2026-01-14

Condition(s) studied

Schizophrenia

Study summary

Schizophrenia is a common, long-term mental illness. It causes problems with thoughts, feelings, and behavior, including positive symptoms (hallucinations, delusions), negative symptoms (lack of emotion, motivation), and cognitive impairment (trouble with thinking, memory, and attention). While antipsychotic drugs effectively treat positive symptoms, they don't help much with cognitive impairment.This study will examine how the tryptophan-kynurenine pathway in the brain contributes to cognitive problems in people having their first episode of schizophrenia and treated with a single antipsychotic. Our goal is to create models for early detection of cognitive impairment in schizophrenia and find potential targets for new treatments to improve thinking and memory.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy volunteers matched to the patient group on sex, age, and education level; * Ethnic Han Chinese; * Able and willing to provide written informed consent. Exclusion Criteria: * Significant comorbid medical or neurological conditions; * Any DSM-5-defined psychiatric disorder; * Family history of psychiatric illness spanning three or more generations; * Current use of psychoactive medications; * Refusal to provide informed consent/participate.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tianjin Anding Hospital Tianjin China

More Tianjin Anding Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07162467 on ClinicalTrials.gov ↗ ← All trials in China