NORCCAP: Norwegian Colorectal Cancer Prevention Trial
Colorectal Cancer, Adenoma
About this trial
This is an interventional prevention trial for Colorectal Cancer focused on measuring screening, flexible sigmoidoscopy, fecal occult blood, cancer, colon, rectum
Eligibility Criteria
Inclusion Criteria: Men and women Living in Oslo or Telemark Age 50-64 years Exclusion Criteria: Patients with previous open colorectal surgery (resections, enterostomies) Individuals in need of long lasting attention and nursing services (somatic or psychosocial reasons, mental retardation) On-going cytotoxic treatment or radiotherapy for malignant disease Severe chronic cardiac or lung disease (NYHA III-IV) Patients with heart valve replacement on life long anticoagulant therapy A coronary event during the last 3 months if having lead to hospitalisation Cerebrovascular accident during the last 3 months Resident abroad
Sites / Locations
- Institute of Population-based Cancer Research
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
No Intervention
Active Comparator
A 1 Intervention arm Flex Sig
B Control arm
A 2 Intervention arm Flex Sig + iFOBT
Randomised from the population registry, age 50-64 years and invited for Flexible Sigmoidoscopy (Flex Sig) screening. Half of invitees are additionally invited to provide a stool sample for fecal occult blood testing (Intervention arm A 2). They are drawn directly from the population registry without prior consent to be randomized - approved by Regional Ethics Committees of South-East Norway..
"No screening group" randomised from population age 50-64 years. As for the active intervention arm, the control group was not informed about being randomized to 'no screening' since 'no screening' was the current usual care (and still is in 2015) in Norway - approved by Regional Ethics Committees of South-East Norway.
Randomised from the population registry, age 50-64 years and invited for Flexible Sigmoidoscopy (Flex Sig) screening plus an immunochemical test for fecal occult blood (iFOBT). As for arms A 1 and B, they are drawn directly from the population registry without prior consent to be randomized.