Multicentre Study for Data Collection, Development, and Evaluation of Novel CRC Screening and Diagnostic Methods

Inclusion Criteria28

• CRC Group
• Signature of the informed consent indicating that the subject accepts to participate in the study and to comply with the requirements and restrictions inherent in this study.
• Subjects aged ≥18 years
• Subject is willing to undergo FOBT test, colonoscopy, and tissue biopsy
• Subject for whom the decision to perform a colonoscopy has been made by the treating physician
• Subject has positive CRC diagnosis according to colonoscopy result
• Covered by a Health Insurance System
• Subject is able to comply with all study procedures
• Control Group with risks and presence of polyps
• Signature of the informed consent indicating that the subject accepts to participate in the study and to comply with the requirements and restrictions inherent in this study.
• Subjects aged ≥18 years
• Otherwise healthy individuals with recognized risk factors for CRC development defined by either heredity and/or obesity and/or smoking and/or excess alcohol consumption and/or hyperlipidaemia.
• Subject be willing to undergo FOBT test, colonoscopy, and tissue biopsy
• Subject has negative CRC diagnosis according to colonoscopy result
• Covered by a Health Insurance System, which will cover colonoscopy as screening in patients with risk factors and alarm symptoms such as abdominal pain, change in stool texture, change in stool frequency, blood in stool/rectal bleeding, diarrhea, constipation, abdominal bloating, weight loss, tiredness.
• Control Group with risks and absence of polyps
• Signature of the informed consent indicating that the subject accepts to participate in the study and to comply with the requirements and restrictions inherent in this study.
• Subjects aged ≥18 years
• Otherwise healthy individuals with recognized risk factors for CRC development defined by either heredity and/or obesity and/or smoking and/or excess alcohol consumption and/or hyperlipidaemia.
• Subject be willing to undergo FOBT test, colonoscopy, and tissue biopsy
• Subject has negative CRC diagnosis according to colonoscopy result
• Covered by a Health Insurance System, which will cover colonoscopy as screening in patients with risk factors and alarm symptoms such as abdominal pain, change in stool texture, change in stool frequency, blood in stool/rectal bleeding, diarrhea, constipation, abdominal bloating, weight loss, tiredness.
• Control Group with no risks
• Signature of the informed consent indicating that the subject accepts to participate in the study and to comply with the requirements and restrictions inherent in this study.
• Subjects aged ≥40 years
• Otherwise healthy individuals without any recognized risk factors for CRC development defined by either heredity and/or obesity and/or smoking and/or excess alcohol consumption and/or hyperlipidemia.
• Subject be willing to undergo FOBT test
• Subject has negative FOBT result