Condition: Screening for Colon Cancer · Blood Samples · Survey and Questionnaire · Sponsor: ADVANCED MARKER DISCOVERY S.L.
The objective of this low-risk interventional study is to evaluate whether the PreveCol® test has sufficient efficiency to be considered as a second-line method for the detection of both colorectal cancer and advanced adenomas when used prospectively in the screening population with a previous positive FOBT result, which could include any of the following: both sexes, age 50-69 years, asympthomatic volunteers. The main aims to be answered are: * Values of efficacy, efficiency, impact and safety of PreveCol. * Values of preferences of participants for screening methods. * Values of PREMs into screening programme. Participants will provide a blood sample prior to a screening colonoscopy, and complete two questionnaires. They will give their sample, information and clinical data to the investigator or health care personnel.
This description comes directly from the study's public registry record.
Marta Jimenez, PhD · +34 637899149 · mjimenez@amadix.com
Always discuss trial participation with your own doctor first.
| Hospital de Santa Maria | Lisbon, Lisbon District, Portugal | Not Yet Recruiting |
| Hospital Universitario Ramon y Cajal | Madrid, Madrid, Spain | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06703632