Clinical trial · Observational
Multi-Omics Noninvasive Inspection of TumOr Risk for Gastric Cancer
Validation of a Plasma-based Multiomics Assay and Risk Scoring Model for Screening of Gastric Malignancies
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a prospective, case-control study intended to develop and validate a blood-based multi-omics assay and computational model for early detection of gastric cancer. Approximately 450 subjects who receive esophageogastroscopy (EGD) will be enrolled and assigned to three arms including gastric cancer, precancerous lesion, and healthy control based on the diagnosis of EGD and histological results. Cell free DNA will be extracted from peripheral blood of all participants and assayed by next-generation sequencing for biomarkers including somatic mutation, methylation, and chromosome instability signals. In the first stage a multi-omics models will be developed for classification between malignancy group and control groups, and between precancerous group and healthy control. Sensitivity and specificity of the model will be evaluated in an independent validation group in the second stage.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ctDNA multi-omics test | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- Gastric cancer group
- interventionNames
- Device: ctDNA multi-omics test
- label
- Precancerous lesion group
- interventionNames
- Device: ctDNA multi-omics test
- label
- Healthy group
- interventionNames
- Device: ctDNA multi-omics test
Primary outcomes (1)
- measure
- The sensitivity and specificity of blood-based multi-omics assay for early detection of gastric cancer with comparison to EGD and/or histological diagnosis.
- timeFrame
- 24 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 40 Years
- Maximum age
- 88 Years
Show eligibility criteria text
Inclusion Criteria: * Age≥40 * Received EGD; * Subjects must have given written informed consent, and the subjects compliance are good. Exclusion Criteria: * Subjects who could not accept EGD; * Subjects who had previously undergone total or partial gastrectomy; * There are other serious acute or chronic medical or mental diseases or laboratory abnormalities that may interfere with the interpretation of the research results and make the subjects unsuitable for the study in the judgment of the researchers; * Subjects with a history of malignant tumor or two or more malignant tumors at the same time; * Pregnant subjects; * Subjects who had a history of bone marrow or organ transplantation, or had a history of blood transfusion one month before enrollment. * The subjects with incomplete clinical data collection or other reasons judged by the researchers are not suitable for this study.
References
Publications (0)
Data not yet available