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Detection of Colorectal Adenomas in Côte-d'Or (DACCOR)

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ClinicalTrials.gov Identifier: NCT02859714
Recruitment Status : Unknown
Verified July 2016 by Centre Hospitalier Universitaire Dijon.
Recruitment status was:  Not yet recruiting
First Posted : August 9, 2016
Last Update Posted : August 9, 2016
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire Dijon

Brief Summary:
Previous studies have shown geographic disparities in the detection of colorectal adenomas in Côte-d'Or, with an impact of the distance from the general practitioner and an ecological deprivation index (EDI). On the other hand, the extremely low detection rates for these lesions in everyday practice before the implementation of organized screening for colorectal cancer in the Côte-d'Or were shown. One of the aims of this screening is to reduce socio-geographic inequalities in access to care and prevention. Yet, participation in screening also varies depending on the socio-economic level. In this context, the Côte-d'Or Polyps Registry, the only body to have data for the pre-screening period (before 2003), will make it possible to determine whether the implementation of organized screening led to the elimination of socio-geographic disparities concerning the detection of adenomas.

Condition or disease Intervention/treatment
Colorectal Adenoma Other: screening data

Study Type : Observational
Estimated Enrollment : 11600 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Detection of Colorectal Adenomas in Côte-d'Or: Impact of Organized Screening on Socio-geographic Disparities
Estimated Primary Completion Date : January 2017

Group/Cohort Intervention/treatment
colorectal adenoma Other: screening data



Primary Outcome Measures :
  1. Detection rates for colorectal adenomas [ Time Frame: through the study completion up to 2 years ]


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Ages Eligible for Study:   50 Years to 74 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients residing in Côte d'Or with a first colorectal adenoma (including in situ carcinomas) diagnosed between 01/01/1997 and 31/12/2008.
Criteria

Inclusion Criteria:

  • The study population will include all patients residing in Côte d'Or with a first colorectal adenoma (including in situ carcinomas) diagnosed between 01/01/1997 and 31/12/2008

Exclusion Criteria:

  • Absence of address
  • history (or suspected history) of previously resected adenoma
  • personal history of colorectal cancer or colorectal cancer discovered in the year following resection of the adenoma (because the cancer was probably not seen at the initial colonoscopy)
  • familial polyposis or known HNPCC
  • chronic inflammatory bowel disease

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02859714


Contacts
Contact: Vanessa COTTET 03.80.39.34.87 ext 33 vanessa.cottet@chu-dijon.fr

Locations
France
CHU Dijon Bourgogne Not yet recruiting
Dijon, France, 21079
Contact: Vanessa COTTET    03.80.39.34.87    vanessa.cottet@chu-dijon.fr   
Sponsors and Collaborators
Centre Hospitalier Universitaire Dijon

Responsible Party: Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier: NCT02859714     History of Changes
Other Study ID Numbers: COTTET PARI 2015
First Posted: August 9, 2016    Key Record Dates
Last Update Posted: August 9, 2016
Last Verified: July 2016

Additional relevant MeSH terms:
Adenoma
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms