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The Northern-European Initiative on Colorectal Cancer

Study acronym: NordICC
StatusActive, Not Recruiting
PhasePhase 3
Started2009-05
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 19, 2017 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2017-06-16
notable
Recruiting→Active, Not Recruiting Study Identification, Study Status, Sponsor/Collaborators, Study Design, Contacts/Locations v4
Trial statusRecruiting→Active, Not Recruiting
Enrollment targetestimated 66000→confirmed 95000
Study sites9→7
Lead sponsorNorwegian Department of Health and Social Affairs→Oslo University Hospital
Collaborators8 to 7 entries
Riga Eastern Clinical University Hospital, Riga, Latvia
2011-06-09
minor
Study Status, Contacts/Locations v3
Study sitesdetails revised at 2 of 9 sites
2010-05-27
minor
Study Status, Study Description, Outcome Measures, Contacts/Locations v2
Secondary endpointsdetails revised at 2 of 2 entries
2009-11-13
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Study sitesdetails revised at 9 of 9 sites
2009-04-17
minor
Original filing
Colorectal cancer (CRC) is a major burden in western countries. The disease develops from precursor lesions during a long time-interval. Colonoscopy can detect and remove CRC precursor lesions and may thus be effective for CRC prevention. Many national and international health organisations demand evidence from randomised trials to reduce incidence or mortality of the target disease before advocating population-wide cancer screening. However, while colonoscopy screening for the prevention of colorectal cancer is established in the United States and several European countries, no randomised trials exist to quantify the possible benefit of colonoscopy screening. NordICC is a randomised trial investigating the effect of colonoscopy on CRC incidence and mortality. NordICC is a multicentre, randomised trial in Nordic countries, the Netherlands and Poland. A minimum of 66 000 individuals, age 55-64 years, are drawn randomly from the population registries in the participating countries. 22 000 are invited for once-only colonoscopy (2:1 randomisation). Expected work-load with 50% compliance will be 11,000 colonoscopies. At the screening examination, all detected lesions are biopsied and removed whenever possible. The remaining 44 000 individuals (control group) are not offered any screening examination (care as usual).The primary study aims are CRC incidence and CRC mortality after 15 years of follow-up, with an interim analysis after 10 years of follow-up. In an intention-to-treat approach, a risk reduction of CRC mortality of 25% in the colonoscopy screening group compared to the control group is expected after 10 years follow-up, estimating 50% compliance in the screening group.
Trial Details
NCT Number NCT00883792
Lead Sponsor Oslo University Hospital
Collaborators: Maria Sklodowska-Curie National Research Institute of Oncology, Erasmus Medical Center, Landspitali University Hospital, Uppsala University Hospital, Karolinska Institutet, Memorial Sloan Kettering Cancer Center, Harvard School of Public Health (HSPH)
Conditions Colorectal Cancer
Enrollment 95,000 participants
Start Date 2009-05
Primary Completion 2026-06 (estimated)
Study Completion 2036-07 (estimated)
Updated on ClinicalTrials.gov 2017-06-19