Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Active, not recruiting Not applicable Interventional Accepts healthy volunteers

Colonoscopy Versus Fecal Immunochemical Test in Reducing Mortality From Colorectal Cancer (CONFIRM)

ClinicalTrials.gov ID: NCT01239082

Public ClinicalTrials.gov record NCT01239082. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 1:14 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CSP #577 - Colonoscopy vs. Fecal Immunochemical Testing in Reducing Mortality From Colorectal Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Colorectal cancer (CRC) is currently the second most common cause of cancer death in the United States, and one of the most preventable cancers. It has been shown in several randomized controlled trials that screening using fecal occult blood testing (FOBT) reduces CRC mortality by 13-33%. While there is strong consensus amongst experts regarding the value of CRC screening, the best approach to screening is not clear. Of the widely recommended modalities, FOBT and colonoscopy are the most commonly used within the United States. FOBT is inexpensive, non-invasive, and its use as a screening tool is supported by the highest quality evidence (i.e. randomized controlled trials). Moreover, newer FOBT, such as fecal immunochemical tests or fecal immunochemical tests (FITs), have advantages over conventional FOBT in terms of both test characteristics and ease of use that make them quite attractive as a population-based screening tool. While colonoscopy is invasive and has higher up-front risks and costs than FOBT, it does afford the opportunity to directly assess the colonic mucosa and is widely believed to be the best test to detect colorectal cancer. In addition, colonoscopy allows for the detection and removal of colorectal adenomas -a well recognized colorectal cancer precursor. There is indirect evidence that suggests colonoscopy is effective in reducing colorectal cancer mortality, but to date, no large clinical trials have been completed to support this assumption. While colonoscopy use is increasing, data is emerging that colonoscopy may not be as effective as previously believed. Prior support for colonoscopy as a screening test relied upon effectiveness estimates that now appear to be overly optimistic. Given the invasive nature of colonoscopy, the associated small, but real risk of complications, and dramatically higher costs than other screening tests, it is especially important to determine the true comparative effectiveness of colonoscopy relative to other proven non-invasive options. The investigators propose to perform a, large, simple, multicenter, randomized, parallel group trial directly comparing screening colonoscopy with annual fecal immunochemical test (FIT) screening in average risk individuals. The hypothesis is that colonoscopy will be superior to FIT in the prevention of colorectal cancer mortality measured over 10 years. Individuals will be enrolled if they are currently eligible for CRC screening (e.g. no colonoscopy in the past 10 years and no FOBT in the past 1 year) and are between 50 and 75 years of age. The investigators will exclude individuals for whom colonoscopy is indicated (e.g. signs or symptoms of CRC, first degree family member with CRC, personal history of colorectal neoplasia or inflammatory bowel disease). All participants will complete baseline demographic, medication, and lifestyle questionnaires (e.g. diet, non-steroidal anti-inflammatory use, frequency of exercise) prior to randomization in a 1:1 ratio to either screening colonoscopy or annual FIT screening (Figure 1). Those testing positive by FIT will undergo evaluation to determine appropriateness for colonoscopy. Screening will be performed in a manner consistent with the currently accepted standard of care in order to determine the comparative effectiveness of the two screening strategies. Participants will be surveyed annually to determine if they have undergone colonoscopy or been diagnosed with CRC. The primary study endpoint will be CRC mortality within 10 years of enrollment. The secondary endpoints are (1) the incidence of CRC within 10 years of enrollment and (2) major complications of colonoscopy. Mortality will be determined through queries of the VA Vital Status File. Cause of death will be determined primarily using death certificates from the National Death Index-Plus database, augmented by adjudication of medical records for known CRC cases where CRC is not listed as a cause of death on the death certificate. The investigators postulate that screening colonoscopy will result in a 40% reduction in CRC mortality over 10 years relative to annual FIT screening. Using a log-rank test with a 2-sided test of significance, =0.05, a sample size of 50,000 participants will be required to test the primary hypothesis with 82% power, assuming a 1% annual rate of crossover from FIT to colonoscopy and a 0.5% annual rate of loss to follow-up. The planned study duration is 12.5 years with 2.5 years of recruitment and 10 years of follow-up for all enrolled participants.

Study identification

NCT ID
NCT01239082
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
50,126 participants

Conditions and interventions

Interventions

Procedure

Eligibility (public fields only)

Age range
50 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2012 (Actual)
Primary completion
Dec 1, 2028 (Estimated)
Completion
Dec 1, 2028 (Estimated)
Last update posted
Sep 4, 2026

2012 – 2028

United States locations

U.S. sites
45
U.S. states
34
U.S. cities
45
Facility City State ZIP Site status
Phoenix VA Health Care System, Phoenix, AZ Phoenix Arizona 85012 —
Central Arkansas Veterans Healthcare System, Little Rock, AR Little Rock Arkansas 72205 —
VA Central California Health Care System, Fresno, CA Fresno California 93703 —
VA Loma Linda Healthcare System, Loma Linda, CA Loma Linda California 92357-1000 —
VA Long Beach Healthcare System, Long Beach, CA Long Beach California 90822 —
VA San Diego Healthcare System, San Diego, CA San Diego California 92161-0002 —
VA Greater Los Angeles Healthcare System, West Los Angeles, CA West Los Angeles California 90073-1003 —
Rocky Mountain Regional VA Medical Center, Aurora, CO Aurora Colorado 80045-7211 —
VA Connecticut Healthcare System West Haven Campus, West Haven, CT West Haven Connecticut 06516-2770 —
Washington DC VA Medical Center, Washington, DC Washington D.C. District of Columbia 20422-0001 —
North Florida/South Georgia Veterans Health System, Gainesville, FL Gainesville Florida 32608-1135 —
Miami VA Healthcare System, Miami, FL Miami Florida 33125 —
Orlando VA Healthcare System, Orlando, FL Orlando Florida 32827 —
James A. Haley Veterans' Hospital, Tampa, FL Tampa Florida 33612 —
Atlanta VA Medical and Rehab Center, Decatur, GA Decatur Georgia 30033-4004 —
VA Pacific Islands Health Care System, Honolulu, HI Honolulu Hawaii 96819-1522 —
Jesse Brown VA Medical Center, Chicago, IL Chicago Illinois 60612 —
Richard L. Roudebush VA Medical Center, Indianapolis, IN Indianapolis Indiana 46202-2884 —
Robley Rex VA Medical Center, Louisville, KY Louisville Kentucky 40206-1433 —
Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD Baltimore Maryland 21201 —
VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Boston Massachusetts 02130-4817 —
VA Ann Arbor Healthcare System, Ann Arbor, MI Ann Arbor Michigan 48105-2303 —
John D. Dingell VA Medical Center, Detroit, MI Detroit Michigan 48201-1916 —
Minneapolis VA Health Care System, Minneapolis, MN Minneapolis Minnesota 55417-2309 —
Kansas City VA Medical Center, Kansas City, MO Kansas City Missouri 64128-2226 —
St. Louis VA Medical Center John Cochran Division, St. Louis, MO St Louis Missouri 63106-1621 —
Manchester VA Medical Center, Manchester, NH Manchester New Hampshire 03104-7007 —
East Orange Campus of the VA New Jersey Health Care System, East Orange, NJ East Orange New Jersey 07018 —
Northport VA Medical Center, Northport, NY Northport New York 11768-2200 —
Durham VA Medical Center, Durham, NC Durham North Carolina 27705-3875 —
Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NC Salisbury North Carolina 28144 —
Louis Stokes VA Medical Center, Cleveland, OH Cleveland Ohio 44106-1702 —
Oklahoma City VA Medical Center, Oklahoma City, OK Oklahoma City Oklahoma 73104-5007 —
VA Portland Health Care System, Portland, OR Portland Oregon 97207-2964 —
Philadelphia MultiService Center, Philadelphia, PA Philadelphia Pennsylvania 19106 —
Providence VA Medical Center, Providence, RI Providence Rhode Island 02908-4734 —
Memphis VA Medical Center, Memphis, TN Memphis Tennessee 38104-2127 —
VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX Dallas Texas 75216-7167 —
Michael E. DeBakey VA Medical Center, Houston, TX Houston Texas 77030-4211 —
VA Salt Lake City Health Care System, Salt Lake City, UT Salt Lake City Utah 84148-0001 —
White River Junction VA Medical Center, White River Junction, VT White River Junction Vermont 05001-3833 —
Richmond VA Medical Center, Richmond, VA Richmond Virginia 23249-0001 —
VA Puget Sound Health Care System Seattle Division, Seattle, WA Seattle Washington 98108-1532 —
Clarksburg Louis A. Johnson VA Medical Center, Clarksburg, WV Clarksburg West Virginia 26301-4155 —
William S. Middleton Memorial Veterans Hospital, Madison, WI Madison Wisconsin 53705-2254 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01239082, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 4, 2026 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01239082 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →