Skip to content

European Polyp Surveillance Trial

Randomized Controlled Trial of Comparison Between Surveillance Intervals After Excision of Colonic Adenomas

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02319928
Acronym
EPoS
Enrollment
20000
Registered
2014-12-18
Start date
2015-06-30
Completion date
2028-12-31
Last updated
2021-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms

Brief summary

This protocol describes the epos (ancient greek (Επος) for story) of a group of related clinical trials aiming at addressing one of the most important unsolved challenges in the prevention of colorectal cancer (one of our major cancer killers); the surveillance of patients with premalignant polyps in the large bowel. This project is timely because large scale colorectal cancer screening programmes are currently rolled out in most Western countries. These programmes are diagnosing large numbers of individuals with premalignant polyps (adenomas and serrated polyps). This creates both a diagnostic and resource dilemma, because the optimal surveillance strategy for these individuals to reduce future cancer risk is currently unknown.. The EPoS trials will randomize or register more than 20,000 individuals in different European countries to different surveillance colonoscopy intervals to disentangle the most effective and cost-effective surveillance strategy for the population. Subjects will be randomized according to their presenting polyp chracteristics The EPoS I trial randomizes patients with low-risk adenomas into 5 or 10-year surveillance; ; EPoS II randomizes patients with high-risk adenomas into 3 or 5-yearly surveillance ; EPoS III will include patients with serrated polyps in a one-arm study with surveillance after 5 and 10 years. The primary endpoint for all three trials is incidence of colorectal cancer after 10 years of follow-up. This EPoS trials are the largest in polyp surveillance ever conducted. They address a clinical problem affecting hundreds of thousand individuals in Europe and the US each year, it has a large size, and should thus provide definitive results.

Interventions

PROCEDUREColonoscopy

Sponsors

Asociación Española de Gastroenterología
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

* Cecal intubation (preferably documented by images/videoof the apendiceal orifice and the ileocecal valve; but not required). * Adequate colonic cleansing, with Boston Bowel Cleansing Score equal or higher than 2 points in all colonic segments. * Complete excision of all polyps at baseline colonoscopy findings (as judged by the trial endoscopists).

Exclusion criteria

* Lack of consent * History of CRC or adenomas * History of serrated polyps ≥ 10 mm in diameter at any colorectal location or ≥ 5 mm if located proximal to the splenic flexure * Incomplete colonoscopy * Incomplete endoscopic excision of polyps * Genetic cancer syndrome (adenomatous or serrated polyposis syndrome; Lynch or Lynch-like syndrome) * Inflammatory bowel disease * History of surgical colon resection for any reason * Severe co-morbidity with reduced life expectancy (NYHA 3-4) * On-going cytotoxic treatment or radiotherapy for malignant disease * Long-lasting attention and nursing services (somatic or psychosocial, mental retardation).

Design outcomes

Primary

MeasureTime frameDescription
Colorectal cancer incidence10 yearsdevelopment of new colorectal cancer cases in the different arms of the trial

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026