Plasma Metabolic Biomarkers for Multi-Cancer Diagnosis
NCT06363123
Summary
The aim of this observational study is to comprehensively analyze the metabolites in plasma samples from multi-cancer patients using advanced mass spectrometry detection technology, in conjunction with metabolomics approaches. The goal is to construct a plasma metabolite database for multi-cancer patients. Simultaneously, we will delve into the exploration and validation of a series of metabolic biomarkers for early multi-cancer diagnosis. The objective is to establish a safer, more convenient, and more sensitive early screening method, thereby providing a reliable scientific foundation and critical evidence for improving the early diagnostic process for individuals at high risk of multi-cancer.
Eligibility
Inclusion Criteria: * Multi-Cancer Group: * Patients with a confirmed diagnosis based on the clinical "gold standard". * Collection of plasma samples prior to treatment. * Availability of complete clinical data. * Control Group: * Individuals with no abnormalities in routine physical examinations and relevant clinical tests. * Age ≥ 45 years. * Availability of complete clinical data. Exclusion Criteria: * Previous reception of anti-tumor treatments (including radiotherapy, chemotherapy, etc.) before blood collection. * Coexistence of other systemic tumors. * Absence of plasma sample collection before treatment. * Pregnancy status. * No clear evidence of histopathological diagnosis (not applicable to the control group based on this criterion). * Patients with severe acute infections. * Patients with severe anemia. * Patients with severe liver or kidney dysfunction. * Patients with autoimmune deficiency diseases. * Patients with Hyperlipidemia. * Patients received contrast agent injection before blood draw. * Patients with psychiatric disorders.
Conditions15
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NCT06363123