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The Norwegian Dietary Guidelines and Colorectal Cancer Survival Study

Study acronym: CRC-NORDIET
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Re-verified, no change to tracked fieldsv6
  2. Study title shortened, about 4 wordsv5
  3. Primary completion date: Mar 2040 to Dec 31, 2034v4 Show 12 more changesShow less
    • Primary endpoints: 5 to 2
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 500 to confirmed 503
    • Study sites: 5 to 3
    • Study completion date: Mar 2040 to Dec 31, 2040
    • Start date: Mar 2012 to Mar 1, 2012
    • Interventions: new norwegian food based dietary guidelines (Other) to Norwegian food based dietary guidelines (Other)
    • Secondary endpoints: 12 to 16
    • Study description expanded, about 45 words
    • Collaborators: 7 to 5
    • Publications: 7 to 9
    • Study title shortened, about 3 words
  4. 2 versions Re-verified since May 2, 2014, no change to tracked fieldsv2-v3
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The current study is designed to gain a better understanding of the role of a healthy diet aimed at dampening inflammation and oxidative stress on long-term disease outcomes and survival in colorectal cancer patients. Since previous research on the role of diet for colorectal cancer survivors is limited, the study may be of great importance for this cancer population.
Trial Details
NCT Number NCT01570010
Lead Sponsor University of Oslo
Collaborators: Oslo University Hospital, Finnish Institute for Health and Welfare, University Hospital, Akershus, Norwegian Cancer Society, The Research Council of Norway
Conditions
(from sponsor)		 Colorectal Cancer
Related terms Colorectal Neoplasms
Enrollment 503 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov