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Colorectal Cancer Screening in Familiar-Risk Population: Immunochemical Fecal Occult Blood Testing Versus Colonoscopy (COLONFAM)

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Immunochemical fecal occult blood test And colonoscopy if test is positive
Colonoscopy with sedation
Sponsored by
Enrique Quintero
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring FOBT, colonoscopy, familiar risk, colorectal cancer, advanced adenoma

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women aged 40-75 years, first degree relatives of patients with non-syndromic CRC

Exclusion Criteria:

  • Personal history of CRC, colorectal adenoma, colorectal polyposis, or inflammatory bowel disease

Sites / Locations

  • Hospital Universitario de Canarias

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Fecal occult blood testing

Colonoscopy

Arm Description

Immunochemical fecal occult blood test Annual (3 rounds), without diet restriction, 1 stool sample. Positive cut-off level: 50 ng/ml.

Colonoscopy with sedation.

Outcomes

Primary Outcome Measures

Advanced colorectal neoplasm detection rate [Time Frame: 2 years] [Designated as safety issue: No]

Secondary Outcome Measures

Complications rate

Full Information

First Posted
February 24, 2010
Last Updated
January 7, 2014
Sponsor
Enrique Quintero
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1. Study Identification

Unique Protocol Identification Number
NCT01075633
Brief Title
Colorectal Cancer Screening in Familiar-Risk Population: Immunochemical Fecal Occult Blood Testing Versus Colonoscopy
Acronym
COLONFAM
Official Title
Colorectal Cancer Screening in Familiar-Risk Population: a Randomized Control Trial Comparing Immunochemical Fecal Occult Blood Testing Versus Colonoscopy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Enrique Quintero

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is aimed: 1) to compare the accuracy of colonoscopy vs immunochemical faecal occult blood test (iFOBT) and colonoscopy when positive for colorectal cancer (CRC) screening in familiar-risk population and; 2) to determine the complications associated with both strategies.
Detailed Description
This is an observational, controlled, randomized phase III study to evaluate the effectiveness of the iFOBT for detecting advanced neoplasia (polyps > 1cm in size, high grade dysplasia or with villous component, or CRC) in first degree relatives of patients with CRC. Index cases will be interviewed to obtain the family tree and their first-degree relatives will be contacted to invite them to participate in the study. Index-cases, will be randomized into one of the following two groups in order that their relatives receive the same screening strategy: A) colonoscopy; or B) annual iFOBT test (OC-Sensor®, cut off ≥50 ng/ml) and colonoscopy if positive. To determine the sensitivity and specificity of the iFOBT strategy, individuals randomized to group B will be invited to undergo a complete colonoscopy following two years follow-up. In addition, epidemiological data, personal history of disease, family history of neoplasm, characteristics of lesions at colonoscopy and histological diagnosis will be recorded. To test the hypothesis of equivalence between the iFOBT test and colonoscopy for detecting advanced colorectal neoplasm, it was considered a probability of participation, detection capability and prevalence of advanced adenomas for iFOBT of 0.750, 0.565 and 0.077, respectively, being the product of them 0.033. In the case of colonoscopy, the likelihood of participation, detection capability and prevalence of advanced adenomas in this population at risk are 0,500, 0.965 and 0.077, respectively, and their product 0.037. Accordingly, for a Type I error (alpha) of 5%, a power of 80% and a maximum deviation between the probabilities of the two tests of 0.03 the number of subjects to be included per arm is 744

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
FOBT, colonoscopy, familiar risk, colorectal cancer, advanced adenoma

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1501 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fecal occult blood testing
Arm Type
Experimental
Arm Description
Immunochemical fecal occult blood test Annual (3 rounds), without diet restriction, 1 stool sample. Positive cut-off level: 50 ng/ml.
Arm Title
Colonoscopy
Arm Type
Active Comparator
Arm Description
Colonoscopy with sedation.
Intervention Type
Procedure
Intervention Name(s)
Immunochemical fecal occult blood test And colonoscopy if test is positive
Intervention Description
Annual (3 rounds), without diet restriction, 1 stool sample. Positive cut-off level: 50 ng/ml.
Intervention Type
Procedure
Intervention Name(s)
Colonoscopy with sedation
Intervention Description
Colonoscopy with sedation
Primary Outcome Measure Information:
Title
Advanced colorectal neoplasm detection rate [Time Frame: 2 years] [Designated as safety issue: No]
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Complications rate
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women aged 40-75 years, first degree relatives of patients with non-syndromic CRC Exclusion Criteria: Personal history of CRC, colorectal adenoma, colorectal polyposis, or inflammatory bowel disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrique Quintero, MD
Organizational Affiliation
Fundación Canaria para la Investigación Biomédica Rafael Clavijo
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Universitario de Canarias
City
Tenerife
ZIP/Postal Code
38320
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
19307978
Citation
Gimeno-Garcia AZ, Quintero E, Nicolas-Perez D, Hernandez-Guerra M, Parra-Blanco A, Jimenez-Sosa A. Screening for familial colorectal cancer with a sensitive immunochemical fecal occult blood test: a pilot study. Eur J Gastroenterol Hepatol. 2009 Sep;21(9):1062-7. doi: 10.1097/MEG.0b013e3283293797.
Results Reference
result
PubMed Identifier
25127679
Citation
Quintero E, Carrillo M, Gimeno-Garcia AZ, Hernandez-Guerra M, Nicolas-Perez D, Alonso-Abreu I, Diez-Fuentes ML, Abraira V. Equivalency of fecal immunochemical tests and colonoscopy in familial colorectal cancer screening. Gastroenterology. 2014 Nov;147(5):1021-30.e1; quiz e16-7. doi: 10.1053/j.gastro.2014.08.004. Epub 2014 Aug 13.
Results Reference
derived

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Colorectal Cancer Screening in Familiar-Risk Population: Immunochemical Fecal Occult Blood Testing Versus Colonoscopy

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