Clinical Trials Detalhe
Advanced GC Multi-omic Characterization in EU and CELAC Populations
General Information
Gender
ALL
Age
from 18 Years to 90 Years
Phase
N/A
Study Type
OBSERVATIONAL
Location
Institute of Pathology and Immunology of University of Porto (Porto, Portugal)
Clinicaltrial.gov
https://classic.clinicaltrials.gov/ct2/show/NCT04015466Summary
Observational study (cohort type) of advanced GC patients that will be recruited prospectively to study biological factors associated with the disease and relevant clinical outcomes.
Conditions
Gastric Cancer
Eligibility
Cases: * Inclusion criteria: * Subjects ≥18 years old. * GC diagnosis stages III and IV (including gastroesophageal junction cancer) and/or a gastroscopy indication due to the high diagnostic suspicion of GC as part of the study of his disease. * Has given and signed the IC to participate in this study. * Exclusion criteria: • Patients diagnosed with GC early disease (stage I and II) suitable for resectable strategy. * Withdrawal criteria: * Patients initially recruited with high suspicion of GC diagnosis but not confirmed by the pathological report. Controls: * Inclusion criteria (only for microbiome analysis): * Subjects ≥18 years old. * Subjects to whom a gastroscopy is indicated within clinical care and is confirmed absent of GC in the same centres will be matched in age (+/- 10 years), gender and pertaining from the same region of the GC case. * Has given and signed the IC to participate in this study. * Exclusion criteria: * Subjects from a different geographic area from the cases. * Patients with high suspicion of GC. * Patients with previous histopathologic diagnosis of peptic (gastric or duodenal) ulcer disease and/or atrophy or intestinal metaplasia. * Patients that have received antimicrobials during the 4 weeks period prior to the endoscopy. * Patients that have received proton pump inhibitors or H2-receptor antagonists, at least 2 weeks prior to the endoscopy