Colorectal Cancer Clinical Trial
Official title:
Polyprev Study: Randomized, Multicenter, Controlled Trial Comparing Fecal Immunochemical Test With Endoscopic Surveillance After Advanced Adenoma Resection in Fecal Immunochemical Test Colorectal Cancer Screening Programs.
NCT number | NCT04967183 |
Other study ID # | POLYPREV |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 1, 2022 |
Est. completion date | June 2035 |
Colorectal cancer (CRC) screening programs have been implemented to reduce the burden of the disease. When an advanced colonic lesions is detected, it is recommended to perform endoscopic surveillance with different intervals between explorations. Although the reduction in CRC incidence, endoscopic surveillance is producing a considerable increase in the number of colonoscopies. However, participation in CRC screening programs based on the fecal immunochemical test (FIT) could be a non inferior alternative to endoscopic surveillance. Based on this hypothesis, the research group have designed a randomized clinical trial within the population CRC screening programs to compare FIT surveillance to endoscopic surveillance in patients with advanced lesions resected.
Status | Recruiting |
Enrollment | 3788 |
Est. completion date | June 2035 |
Est. primary completion date | June 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 50 Years to 65 Years |
Eligibility | Inclusion Criteria: 1. Individuals aged 50 to 65 years. 2. Individuals with at least one advanced adenoma (tubulovillous or villous histology, high grade dysplasia or = 10mm), and / or at least three non-advanced adenomas detected and resected completely within the population-based CRC screening program. Exclusion Criteria: 1. Personal history of CRC. 2. Colonic lesion =10mm resected without histological diagnosis. 3. More than 10 adenomas in baseline colonoscopy. 4. Serrated polyposis syndrome. 5. Two or more first-degree relatives with CRC. 6. Hereditary predisposition to CRC. 7. Relevant comorbidity with life expectancy inferior to 5 years. 8. Colonoscopy with incomplete mucosal examination. 9. Incomplete resection of baseline lesions. 10. Non-acceptance after reading the informed consent. |
Country | Name | City | State |
---|---|---|---|
Spain | Complexo Hospitalario Universitario de Ourense | Ourense |
Lead Sponsor | Collaborator |
---|---|
Fundacin Biomedica Galicia Sur |
Spain,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of invasive CRC | It is the main outcome of the study. Invasive CRC is defined as colonic adenocarcinoma that invades the submucosa. Adenocarcinomas in situ and intramucosal carcinomas will not be considered as invasive CRC. | 10 years | |
Primary | Rate of interval CRC | Interval CRC is defined as the CRC detected between two organized surveillance (FIT or colonoscopy). | 10 years | |
Primary | Mortality | The deaths and their cause will be collected: associated with CRC, associated with adverse effects of screening or unrelated. | 10 years | |
Primary | Rate of advanced colonic lesions | Advanced colonic lesions will be defined as advanced adenomas (at least 10mm, hairy histology or high grade dysplasia) or advanced serrated lesions (at least 10mm or with dysplasia). | 10 years | |
Primary | Frequency of participation in the surveillance strategy | According to the methodology of the information systems of the screening programs, three categories will be defined: non-participation, irregular participation, regular participation. | 10 years | |
Primary | Adverse effects | Adverse effects associated with surveillance are defined as complications that require hospitalization. Those related to the surgical treatment of benign colonic lesions will be included as adverse effects. | 10 years | |
Secondary | CRC, adenoma and advanced serrated lesions at three years | Detection of CRC, adenoma and advanced serrated lesion will be collected at 3 years of follow-up. | 3 years | |
Secondary | Physical activity | We will use the International Physical Activity. Questionnaire (IPAQ) to mesure physical activity. | 3 years | |
Secondary | Mediterranean lifestyle | We will use the Mediterranean Lifestyle index (MEDLIFE) to measure overall adherence to the Mediterranean lifestyle. | 3 years | |
Secondary | Preferences of the subjects | We will use a survey with vignette questions to evaluate the values and preferences of the subjects regarding surveillance. | 2 years |
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