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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02289053
Other study ID # K24-DK
Secondary ID 1K24DK084208
Status Completed
Phase N/A
First received February 26, 2014
Last updated May 12, 2017
Start date April 1, 2006
Est. completion date June 30, 2014

Study information

Verified date May 2017
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Conflicting guideline recommendations for screening colonoscopy result due to scant data upon which to develop appropriate recommendations. No previous study has compared the prevalence of advanced adenomas or adenomas (any size) among 40-49 year old individuals with a first degree relative (FDR) with colorectal cancer (CRC) versus 40-49 year old average risk individuals with no family history of CRC. The purpose of this study is to determine the prevalence of colon adenomas in 40-49 year old individuals and identify risk factors associated with the presence of advanced adenomas. This data will provide evidence to determine appropriate colon cancer screening guidelines in 40-49 year old persons with a family history of colon polyps or colorectal cancer.


Recruitment information / eligibility

Status Completed
Enrollment 1623
Est. completion date June 30, 2014
Est. primary completion date June 30, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 49 Years
Eligibility Inclusion Criteria:

- 40-49 year old asymptomatic men and women referred for colorectal cancer screening with a family history of CRC in a first degree relative;

- 40-49 year old asymptomatic men and women referred for colorectal cancer screening with a family history of polyps in a first degree relative;

- 40-49 year old men and women without a family history of CRC or polyps in a first degree relative who are referred for colonoscopy to evaluate scant hematochezia characterized as red blood on toilet tissue after wiping or small droplets of blood on stool or in toilet water after evacuating stool, abdominal discomfort or altered bowel habits characterized as constipation or diarrhea.

Exclusion Criteria:

- Personal history of iron deficiency anemia within six months of referral;

- Personal history of iron deficiency without anemia within six months of referral;

- Personal history of (+) FOBT within one year of referral;

- Personal history of previous colonoscopy or barium enema within the past 10 years;

- Personal history of previous flexible sigmoidoscopy in the past 5 years;

- Personal history of adenoma, colorectal cancer, inflammatory bowel disease, HNPCC, or familial adenomatous polyposis (FAP);

- Unintentional weight loss > 10 lbs within the previous six months;

- Individuals with family history of CRC AND scant hematochezia;

- Inability to speak and read English.

Study Design


Locations

Country Name City State
United States Ann Arbor VA Healthcare System Ann Arbor Michigan
United States University of Michigan Ann Arbor Michigan
United States Walter Reed National Military Medical Center Bethesda Maryland
United States John D. Dingell VA Medical Center Detroit Michigan
United States Durham VA Medical Center Durham North Carolina
United States Huron Gastro Ypsilanti Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Risk factors associated with the presence of advanced adenomas Logistic regression will be used to determine if specific risk factors are associated with the risk of adenomas in 40-49 year old individuals. Data will be collected from patient surveys and medical records. Data analysis will begin September 2014 for a duration of three months.
Primary Prevalence of advanced adenomas among 40-49 year old individuals with and without a family history of colorectal cancer The outcome will be assessed after the completion of patient recruitment at all locations in August 2014. Advanced adenomas are defined as greater than or equal to 10 mm (1 cm). The presence of adenomas is determined be reviewing patient medical records and pathology reports. Data analysis will begin September 2014 for a duration of three months.
Secondary Absolute prevalence of advanced adenomas in 40-49 year olds with a family history of colorectal cancer The outcome will be assessed after the completion of patient recruitment at all locations in August 2014. Advanced adenomas are defined as greater than or equal to 10 mm (1 cm). The presence of adenomas is determined be reviewing patient medical records and pathology reports. Data analysis will begin September 2014 for a duration of three months.
Secondary Absolute prevalence of advanced adenomas in 40-49 year old individuals with a family history of colorectal polyps The outcome will be assessed after the completion of patient recruitment at all locations in August 2014. Advanced adenomas are defined as greater than or equal to 10 mm (1 cm). The presence of adenomas is determined be reviewing patient medical records and pathology reports. Data analysis will begin September 2014 for a duration of three months.
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