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About
Recruit of healthy, precancer and colorectal cancer patients and record necessary information of demographic and also other messages. All the volunteers were asked to provide samples including stool, blood, urine and tissues. This protocol is performed with the permission of the ethics committee and all the participants were provided with informed consent.
Full description
Healthy subjects, precancer patients identified by colonoscopy or colonoscopy history and colorectal cancer patients identified by two independent pathologists will be enrolled. The demographic message including age, weight, height, drug history, family history of all participants will be recorded. Blood, stool and urine samples will be collected of all subjects. Tumor and adjacent tissue samples of colorectal cancer and precancer patients were collected, as well as normal tissue of healthy subjects.
Enrollment
Sex
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Volunteers
Inclusion and exclusion criteria
Inclusion Criteria
Exclusion Criteria:
2,000 participants in 3 patient groups
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Central trial contact
Huanlong Qin, Ph.D
Data sourced from clinicaltrials.gov
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