Actively Recruiting

Phase Not Applicable
Age: 40Years - 75Years
All Genders
NCT06983639

Randomized Trial Comparing Fecal Testing (FIT) to Colonoscopy for Post-polypectomy Surveillance

Led by Sorlandet Hospital HF · Updated on 2026-01-15

4000

Participants Needed

1

Research Sites

1251 weeks

Total Duration

On this page

Sponsors

S

Sorlandet Hospital HF

Lead Sponsor

S

Sykehuset Ostfold

Collaborating Sponsor

AI-Summary

What this Trial Is About

From observational studies, it is know that the risk of developing colorectal cancer after polyp removal is lower if the patients adheres to surveillance recommendations. However, colonoscopy is burdensome for patients and colonoscopy availability is limited in many parts of the world. In addition, more than half of surveillance colonoscopies are without any findings. The trial investigates whether surveillance using fecal testing for blod is as good as colonoscopy after removal of colorectal polyps.

CONDITIONS

Official Title

Randomized Trial Comparing Fecal Testing (FIT) to Colonoscopy for Post-polypectomy Surveillance

Who Can Participate

Age: 40Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • High-quality baseline colonoscopy with adequate cleansing and cecal intubation
  • Removal of at least one advanced adenoma
  • Clean colon with all polyps removed
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Colorectal cancer
  • History of surgical colon resection for any reason
  • Genetic cancer syndrome such as adenomatous or serrated polyposis syndrome, Lynch or Lynch-like syndrome
  • Ten or more adenomas at baseline colonoscopy (cumulative)
  • History of advanced serrated lesion (sessile serrated lesion ≥10mm or with dysplasia)
  • Inflammatory bowel disease
  • Receiving ongoing palliative care for any reason

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sørlandet sykehus HF

Arendal, Agder, Norway, 4838

Actively Recruiting

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Research Team

Ø

Øyvind Holme

CONTACT

M

Michael Bretthauer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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