Colorectal Polyp Clinical Trial
Official title:
Comparative Analysis of the Effects of UNICLA-A2 Against Conventional Dairy Products Administered Daily in Patients at High-risk Colorectal Cancer Development Who Have Undergone Polypectomy
Dietary intervention with UNICLA-A2 milk products containing beta casein A2 protein, and higher levels of omega-3 fatty acids and selenium may contribute to maintain the intestinal integrity, reduce inflammatory processes, normalize the immune system, protect against oxidative damage and equilibrate the gut microbiota in high-risk colorectal cancer patients who have undergone polypectomy
Status | Recruiting |
Enrollment | 34 |
Est. completion date | February 15, 2026 |
Est. primary completion date | May 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Participants diagnosed with high-risk polyps in the colorectal cancer screening programme or in the relative's colon cancer prevention program or patients who are in follow-up due to prior detection of polyps with any of the following characteristics: - At least 10 adenomas - At least 5 proximal serrated polyps (PSP) - At least 2 serrated polyps with diameters =10 mm - Serrated Polyposis Syndrome (SPS) - Early invasive CRC (stage pT1) endoscopically resected (surgery not required) - A sessile or flat lesion = 20 mm with fragmented resection - Patients with previous resection of polyps in which the resection margin was not assessable and are considered susceptible to repeat colonoscopy 2. Regular consumer of milk and dairy products. 3. Informed consent form signed. Exclusion Criteria: 1. History of allergic reaction attributed to compounds of similar chemical composition to the study agents. 2. Incomplete colonoscopy or with poor quality criteria, Boston <6. 3. Concomitant acetylsalicylic acid (ASA), NSAIDs, misoprostol, corticosteroids or statins needed on a regular or predictable basis during the time of the study. 4. Previous gastrointestinal surgery (colon or small intestine or gastric) that affects the absorption of nutrients. 5. History of familial adenomatous polyposis. |
Country | Name | City | State |
---|---|---|---|
Spain | Angel Lanas Arbeloa | Zaragoza |
Lead Sponsor | Collaborator |
---|---|
Instituto de Investigación Sanitaria Aragón | Cooperativas Lacteas Unidas, Hospital Clínico Universitario Lozano Blesa |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline levels in pro-inflammatory circulating markers C-reactive protein (CRP), interleukin (IL)-6, macrophage inhibitory cytokine 1 (MIC-1) and tumour necrosis factor alpha (TNFa), as well as in fecal calprotectin. | The C-reactive protein and calprotectin are measured by conventional methods in the University Clinic Hospital Lozano Blesa and the circulating biomarkers IL-6, MIC-1 and TNFa by enzyme-linked immunosorbent assay | At baseline, at 3 months and through study completion, an average of 1 year after the colonoscopy that motivated the patient´s inclusion | |
Secondary | Change from baseline in fecal microbiota. | Stool samples are collected for DNA extraction and ulterior metagenomic analysis of the fecal microbiota's composition. Library construction is carried out with the Ion 16S™ Metagenomics Kit which permits PCR amplification of hypervariable regions of the 16S rDNA gene from bacteria and the material obtained is subjected to next-generation sequencing (NGS) to see the proportions of the main groups of microorganisms in the sample. | At baseline, at 3 months and through study completion, an average of 1 year after the colonoscopy that motivated the patient´s inclusion | |
Secondary | To assess the effect of treatment on colorectal adenoma recurrence | The number of participants in each arm who develop one or more colorectal adenomas is determined in the follow-up colonoscopy (adenoma detection rate), as well as the presence of advanced or not advanced adenomas, serrated polyps, subtype, location and the total number of adenomas per participant. | Through study completion, an average of 1 year after the initial colonoscopy that motivated the suitability of patients inclusion. |
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