CClinicalTrials.gg
RecruitingNCT05080673FORTEUpdated Sep 2, 2026

Five or Ten Year Colonoscopy for 1-2 Non-Advanced Adenomatous Polyps

An interventional study of 5-year and 10 Year Surveillance Colonoscopy after Qualifying Colonoscopy in Adenocarcinoma of the Colon and Adenocarcinoma of the Rectum, sponsored by NRG Oncology. Recruiting at 493 sites in 2 countries. Open to participants aged 45 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-09-02.

Sponsored by NRG Oncology · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
9,500
Allocation
Randomized
Ages
45 Years to 70 Years
Sex
All
01

Study summary

This trial examines colorectal cancer incidence in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.

Read the detailed description

Colorectal cancer (CRC) is the fourth most common cancer and the second leading cause of cancer death among men and women in the United States (US). The lifetime risk of colorectal cancer in both men and women in the US is approximately 6%. About 93% of colorectal cancer (CRC) diagnoses are in patients older than 50 years (Siegel 2014). Randomized controlled trials show that screening for CRC significantly decreases CRC incidence and mortality (Schoen 2012, Atkin 2010, Mandel 1999, Mandel 2000). CRC screening has received a Grade A recommendation from the US Preventive Services Task Force.

In the U.S., colonoscopy is the most utilized screening modality for CRC. On a population basis, screening rates, which were around 40-50%, have now increased to 65%, and a goal to increase to 80% compliance is being promoted (CDC 2011, CDC 2013, Meester 2015).

Adenomatous polyps are the acknowledged precursors of colorectal cancer. Identification and removal of adenomas is the mechanism by which screening is effective in reducing CRC incidence and subsequent mortality. "Advanced" adenomas are adenomas which are greater than or equal to 1 cm, or have a "villous" component (tubulovillous or villous), or have foci of high grade dysplasia. Advanced adenomas are associated with increased long-term risk of cancer, even years after colonoscopy (Click 2018). The prevalence of advanced adenomas at screening colonoscopy is 5-10% (Ferlitsch 2011, Imperiale 2014). Non-advanced adenomas are adenomas greater than 1 cm with neither villous components nor high grade dysplasia. Non-advanced adenomas are much more common than advanced adenomas, present in around 30% of colonoscopy exams (Ferlitsch 2011, Imperiale 2014).

After detection of adenomas, patients are advised to return periodically for surveillance colonoscopy. Patients with 1-2 non-advanced adenomas are recommended by guidelines to return in 5 - 10 years for follow-up surveillance colonoscopy (Lieberman 2012). However, there are no guidelines on how to triage individuals to 5 as opposed to 10 years. Furthermore, there is limited evidence supporting the effectiveness of surveillance colonoscopy in reducing CRC incidence. A retrospective study in patients with advanced adenomas demonstrated benefit (Atkin 2017), but the study was not randomized and did not include patients with 1-2 non-advanced adenomas. The only randomized trial of surveillance colonoscopy was reported in the early 1990's, when participants were randomized to 3 vs. 1- and 3- year surveillance (Winawer 1993). No difference in advanced adenoma detection was observed when comparing participants examined at the two screening intervals, and as a result, guidelines were modified with participants advised to return every 3 years after adenomatous polyp detection. The recommended interval for non-advanced adenomas was gradually lengthened to the current standard, but there is no randomized, controlled data to support that interval. Furthermore, observational data of surveillance colonoscopy practice in the U.S. demonstrate that recommended intervals are often not adhered to, and individuals return for repeat testing well ahead of guideline recommendations (Schoen 2010, Lieberman 2014).

Furthermore, if anything, retrospective, natural history studies of non-advanced adenomas do not support the association of non-advanced adenoma with a higher risk of subsequent colorectal cancer (Atkin 1992, Spencer 1984, Loberg 2014). For example, in a classic study from the United Kingdom, patients with small rectosigmoid adenomas, even if multiple, did not have an increased risk of CRC compared to the general population, over a 14-year mean follow-up time (Atkin 1992). In a recent observational study from Norway, participants with a low-risk adenoma followed over a median of 7.7 years (maximum 19 years) without subsequent surveillance colonoscopy, had a lower CRC mortality than the general population (Loberg 2014), implying that although the initial colonoscopy may be protective, subsequent follow-up colonoscopy was not required. More recently, several studies have reported that individuals with non-advanced adenomas do not have an increased risk of colorectal cancer compared to those with no adenomas (Click 2018, Lieberman 2019, Lee 2019).

Another recent major development affecting screening is that practitioners of colonoscopy are now recommended to monitor and insure their adenoma detection rates are high. Data from Poland (Kaminski 2010) and Kaiser Permanente in California (Corley 2014) have demonstrated that a higher adenoma detection rate (ADR) is associated with a lower long-term risk of interval CRC, or cancer occurring after colonoscopy. Our understanding of these observations is premised on the notion that leaving pre-neoplastic tissue (adenomas) in situ, (such as what occurs with a lower ADR), increases the chance that an adenoma left behind will subsequently transform into cancer. The concern over interval cancers has stimulated quality concerns about the practice of colonoscopy. Guidelines for a recommended ADR at screening colonoscopy are rising, from the initial targets of 15% in women and 25% in men (Lieberman 2012) to 20% in women and 30% in men or 25% overall. ADRs in clinical studies are now commonly over 30% and some practitioners report rates exceeding 50%. However, adenomas that are detected when the ADR is high or as it increases over time are generally small, non-advanced adenomas.

Current clinical practice favoring colonoscopy-based screening with increased emphasis on detection of adenomas, most of which will turn out to be small, non-advanced adenomas, will greatly increase demand for utilization of surveillance colonoscopy exams in the coming decades. Yet, the evidence for determining the benefit, optimal timing, and recommended frequency of surveillance colonoscopy is unknown. A randomized, clinical trial to demonstrate the difference in yield between 5- or 10-year surveillance for participants with non-advanced adenoma is needed to guide clinical practice. Only a randomized trial will be authoritative enough to define good clinical practice and directly influence clinical care.

02

Conditions studied

  • Adenocarcinoma of the Colon
  • Adenocarcinoma of the Rectum
03

Who can participate

Ages eligible
45 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • The participant must have signed and dated an IRB-approved consent form that conforms to federal and institutional guidelines.
  • Participants greater than or equal to 45 and less than 70 years of age at the time of colonoscopy.
  • Participants with a first-time diagnosis of 1-2 non-advanced tubular adenomas (less than 10 mm without tubulovillous or villous changes or high grade or severe dysplasia) from the qualifying colonoscopy within 4 years prior to randomization.
  • Sessile serrated polyps/adenomas, as long as they do not meet the criteria for advanced adenomas, will be considered as non-advanced adenomas.
  • Qualifying colonoscopy must be a complete colonoscopy with visualization of the cecum and with adequate cleansing within 4 years prior to randomization.
  • Complete excision of all observed polyps in qualifying colonoscopy
  • Participants must be able to read or understand English or Spanish.

Exclusion criteria

Exclusion Criteria:

    • Prior history of colorectal cancer or colorectal adenomas including sessile serrated polyps/adenomas excluding those found on the qualifying colonoscopy.

      • Prior history of a hyperplastic polyp measuring greater than or equal to 1 cm in size.
      • Traditional serrated adenomas found on the qualifying colonoscopy.
      • Hyperplastic polyp measuring greater than or equal to 1 cm in size found on the qualifying colonoscopy.
      • Previous malignancies unless the patient has been disease-free for 5 or more years prior to randomization and is deemed by the physician to be at low risk for recurrence. Patients with the following cancers are eligible if diagnosed and treated within the past 5 years: all in situ cancers and basal cell and squamous cell carcinoma of the skin.
      • Colonoscopy performed after the qualifying colonoscopy but prior to randomization.
      • Incomplete qualifying colonoscopy (e.g., cecum not visualized).
      • Incomplete endoscopic excision of adenomatous polyps based on colonoscopist impression at qualifying colonoscopy. (Excision of all hyperplastic rectosigmoid polyps is not required.)
      • Sub-total colectomy or total proctocolectomy. (Segmental resections are allowed.)
      • Family history of CRC diagnosed at less than or equal to 60 years of age in a first degree relative (mother, father, child, sibling) or in two first degree relatives with CRC at any age.
      • Participants with a clinical diagnosis of a significant heritable risk for colorectal cancer (Familial Adenomatous Polyposis, Hereditary Nonpolyposis Colorectal Cancer [Lynch Syndrome]).
      • Participants tested positive for a Familial Adenomatous Polyposis, Hereditary Nonpolyposis Colorectal Cancer [Lynch Syndrome] genetic mutation that increases risk of colorectal cancer.
      • Inflammatory bowel disease (e.g., Crohn's Disease, ulcerative colitis).
      • Life expectancy less than 10 years due to comorbid conditions in the opinion of the investigator.
      • Other comorbid conditions that would prevent the participant from having colonoscopies or would prevent required follow-up.
04

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
9,500 participants (estimated)

Study arms

  • Experimental
    Arm 1

    5-Year and 10-Year Surveillance Colonoscopy after Qualifying Colonoscopy

    Procedure: 5-year and 10 Year Surveillance Colonoscopy after Qualifying Colonoscopy

  • Experimental
    Arm 2

    10-Year Surveillance Colonoscopy after Qualifying Colonoscopy

    Procedure: 5-year and 10 Year Surveillance Colonoscopy after Qualifying Colonoscopy

Interventions

  • Procedure5-year and 10 Year Surveillance Colonoscopy after Qualifying Colonoscopy

    The five- and ten-year colonoscopies, in addition to any unscheduled colonoscopies, will be performed according to currently accepted guidelines for the performance of quality colonoscopy. Participants will be given the standardized colonoscopy preparation instructions per institutional standards.

05

What researchers measure

Primary outcomes

  1. Incidence of colorectal cancer

    To examine colorectal cancer incidence in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.

    Time frame: 10 years

Other outcomes

  1. Incidence of advanced adenoma

    To examine advanced adenoma incidence in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.

    Time frame: 10 years

  2. Colorectal cancer mortality

    To examine colorectal cancer mortality in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.

    Time frame: 10 years

  3. Incidence of stage III-IV colorectal cancer

    To examine stage III-IV colorectal cancer incidence in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.

    Time frame: 10 years

06

Study locations

343 of 493 sites recruiting
  • Fairbanks Memorial Hospital
    Fairbanks, Alaska 99701, United States
    Active, not recruiting
  • CTCA at Western Regional Medical Center
    Goodyear, Arizona 85338, United States
    • Site Public Contact · Contact · 623-207-3000
    • Arjun Gupta · Principal investigator
    Recruiting
  • Kingman Regional Medical Center
    Kingman, Arizona 86401, United States
    • Site Public Contact · Contact · research@sncrf.org · 702-384-0013
    • John A. Ellerton · Principal investigator
    Recruiting
  • Cancer Center at Saint Joseph's
    Phoenix, Arizona 85004, United States
    Recruiting
  • University of Arizona Cancer Center - Prevention Research Clinic
    Tucson, Arizona 85719, United States
    • Site Public Contact · Contact · pcarino@arizona.edu · 520-318-7057
    • Joshua E. Melson · Principal investigator
    Recruiting
  • Mercy Hospital Fort Smith
    Fort Smith, Arkansas 72903, United States
    • Site Public Contact · Contact · 800-378-9373
    • Jay W. Carlson · Principal investigator
    Recruiting
  • CHI Saint Vincent Cancer Center Hot Springs
    Hot Springs, Arkansas 71913, United States
    Suspended
  • CARTI Cancer Center
    Little Rock, Arkansas 72205, United States
    • Site Public Contact · Contact · Research@CARTI.com · 501-906-4199
    • Jay W. Carlson · Principal investigator
    Recruiting
  • Kaiser Permanente-Anaheim
    Anaheim, California 92806, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Mission Hope Medical Oncology - Arroyo Grande
    Arroyo Grande, California 93420, United States
    Recruiting
  • PCR Oncology
    Arroyo Grande, California 93420, United States
    • Site Public Contact · Contact · research@sncrf.org · 702-384-0013
    • John A. Ellerton · Principal investigator
    Recruiting
  • Kaiser Permanente-Baldwin Park
    Baldwin Park, California 91706, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente-Bellflower
    Bellflower, California 90706, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Mercy Cancer Center - Carmichael
    Carmichael, California 95608, United States
    Recruiting
  • Mercy San Juan Medical Center
    Carmichael, California 95608, United States
    Recruiting
  • Epic Care-Dublin
    Dublin, California 94568, United States
    Active, not recruiting
  • Mercy Cancer Center - Elk Grove
    Elk Grove, California 95758, United States
    Recruiting
  • Bay Area Breast Surgeons Inc
    Emeryville, California 94608, United States
    Active, not recruiting
  • Epic Care Partners in Cancer Care
    Emeryville, California 94608, United States
    Active, not recruiting
  • Kaiser Permanente-Fontana
    Fontana, California 92335, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente South Bay
    Harbor City, California 90710, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente-Irvine
    Irvine, California 92618, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente Los Angeles Medical Center
    Los Angeles, California 90027, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente West Los Angeles
    Los Angeles, California 90034, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • UCLA / Jonsson Comprehensive Cancer Center
    Los Angeles, California 90095, United States
    • Site Public Contact · Contact · 888-798-0719
    • Folasade P. May · Principal investigator
    Recruiting
  • Contra Costa Regional Medical Center
    Martinez, California 94553-3156, United States
    • Site Public Contact · Contact · 925-957-5400
    • Lili X. Wang · Principal investigator
    Recruiting
  • Mercy Cancer Center
    Merced, California 95340, United States
    Recruiting
  • Alta Bates Summit Medical Center - Summit Campus
    Oakland, California 94609, United States
    Suspended
  • Bay Area Tumor Institute
    Oakland, California 94609, United States
    Active, not recruiting
  • Kaiser Permanente-Ontario
    Ontario, California 91761, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Stanford Cancer Institute Palo Alto
    Palo Alto, California 94304, United States
    Recruiting
  • Kaiser Permanente - Panorama City
    Panorama City, California 91402, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente-Riverside
    Riverside, California 92505, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Mercy Cancer Center - Rocklin
    Rocklin, California 95765, United States
    Recruiting
  • Mercy Cancer Center - Sacramento
    Sacramento, California 95816, United States
    Recruiting
  • Kaiser Permanente-Rio San Diego
    San Diego, California 92108, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Kaiser Permanente-San Diego Zion
    San Diego, California 92120, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Pacific Central Coast Health Center-San Luis Obispo
    San Luis Obispo, California 93401, United States
    Recruiting
  • Kaiser Permanente-San Marcos
    San Marcos, California 92078, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Mission Hope Medical Oncology - Santa Maria
    Santa Maria, California 93444, United States
    Recruiting
  • Saint Joseph's Medical Center
    Stockton, California 95204, United States
    • Site Public Contact · Contact · 209-461-5257
    • Shahzad Siddique · Principal investigator
    Recruiting
  • Kaiser Permanente-Vallejo
    Vallejo, California 94589, United States
    • Site Public Contact · Contact · Kpoct@kp.org · 877-642-4691
    • Douglas A. Corley · Principal investigator
    Recruiting
  • Epic Care Cyberknife Center
    Walnut Creek, California 94597, United States
    Active, not recruiting
  • BASS Medical Group - Lennon
    Walnut Creek, California 94598, United States
    Active, not recruiting
  • Woodland Memorial Hospital
    Woodland, California 95695, United States
    Recruiting
  • Kaiser Permanente-Woodland Hills
    Woodland Hills, California 91367, United States
    • Site Public Contact · Contact · clinical.trials@kp.org · 800-398-3996
    • Ahmed I. Megahed · Principal investigator
    Recruiting
  • Rocky Mountain Cancer Centers-Aurora
    Aurora, Colorado 80012, United States
    Active, not recruiting
  • Rocky Mountain Regional VA Medical Center
    Aurora, Colorado 80045, United States
    • Site Public Contact · Contact · 888-336-8262
    • Jessica D. McDermott · Principal investigator
    Recruiting
  • UCHealth University of Colorado Hospital
    Aurora, Colorado 80045, United States
    • Site Public Contact · Contact · 720-848-0650
    • Swati G. Patel · Principal investigator
    Recruiting
  • Boulder Community Foothills Hospital
    Boulder, Colorado 80303, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers-Boulder
    Boulder, Colorado 80304, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers - Centennial
    Centennial, Colorado 80112, United States
    Active, not recruiting
  • Penrose-Saint Francis Healthcare
    Colorado Springs, Colorado 80907, United States
    Recruiting
  • Rocky Mountain Cancer Centers-Penrose
    Colorado Springs, Colorado 80907, United States
    Recruiting
  • Saint Francis Cancer Center
    Colorado Springs, Colorado 80923, United States
    Recruiting
  • Kaiser Permanente-Franklin
    Denver, Colorado 80205, United States
    Recruiting
  • The Women's Imaging Center
    Denver, Colorado 80209, United States
    Active, not recruiting
  • AdventHealth Porter
    Denver, Colorado 80210, United States
    Suspended
  • Colorado Blood Cancer Institute
    Denver, Colorado 80218, United States
    Active, not recruiting
  • Presbyterian - Saint Lukes Medical Center - Health One
    Denver, Colorado 80218, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers-Midtown
    Denver, Colorado 80218, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers-Rose
    Denver, Colorado 80220, United States
    Active, not recruiting
  • CommonSpirit Cancer Center Mercy
    Durango, Colorado 81301, United States
    Recruiting
  • Mercy Medical Center
    Durango, Colorado 81301, United States
    Recruiting
  • Mountain Blue Cancer Care Center - Swedish
    Englewood, Colorado 80113, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers - Swedish
    Englewood, Colorado 80113, United States
    Active, not recruiting
  • The Melanoma and Skin Cancer Institute
    Englewood, Colorado 80113, United States
    Active, not recruiting
  • Kaiser Permanente-Rock Creek
    Lafayette, Colorado 80026, United States
    Recruiting
  • CommonSpirit Saint Anthony Hospital Cancer Center
    Lakewood, Colorado 80228, United States
    Recruiting
  • Rocky Mountain Cancer Centers-Lakewood
    Lakewood, Colorado 80228, United States
    Active, not recruiting
  • Rocky Mountain Cancer Centers-Littleton
    Littleton, Colorado 80120, United States
    Active, not recruiting
  • AdventHealth Littleton
    Littleton, Colorado 80122, United States
    Suspended
  • Kaiser Permanente-Lone Tree
    Lone Tree, Colorado 80124, United States
    Recruiting
  • Rocky Mountain Cancer Centers-Sky Ridge
    Lone Tree, Colorado 80124, United States
    Active, not recruiting
  • Longmont United Hospital
    Longmont, Colorado 80501, United States
    Recruiting
  • Rocky Mountain Cancer Centers-Longmont
    Longmont, Colorado 80501, United States
    Active, not recruiting
  • AdventHealth Parker
    Parker, Colorado 80138, United States
    Suspended
  • Saint Mary Corwin Medical Center
    Pueblo, Colorado 81004, United States
    Recruiting
  • Rocky Mountain Cancer Centers-Thornton
    Thornton, Colorado 80260, United States
    Active, not recruiting
  • Saint Anthony North Hospital
    Westminster, Colorado 80023, United States
    Recruiting
  • Yale-New Haven Hospital Saint Raphael Campus
    New Haven, Connecticut 06511, United States
    Not yet recruiting
  • Yale University
    New Haven, Connecticut 06520, United States
    Recruiting
  • Yale-New Haven Hospital North Haven Medical Center
    North Haven, Connecticut 06473, United States
    Not yet recruiting
  • Veterans Affairs Connecticut Healthcare System-West Haven Campus
    West Haven, Connecticut 06516, United States
    • Site Public Contact · Contact · 203-937-3421
    • Petr Protiva · Principal investigator
    Recruiting
  • Kaiser Permanente-Capitol Hill Medical Center
    Washington D.C., District of Columbia 20002, United States
    Recruiting
  • MedStar Georgetown University Hospital
    Washington D.C., District of Columbia 20007, United States
    • Site Public Contact · Contact · 202-444-2223
    • Priyanka Kanth · Principal investigator
    Recruiting
  • George Washington University Medical Center
    Washington D.C., District of Columbia 20037, United States
    • Site Public Contact · Contact · 202-741-2210
    • Matthew Ng · Principal investigator
    Recruiting
  • Mount Sinai Comprehensive Cancer Center at Aventura
    Aventura, Florida 33180, United States
    • Site Public Contact · Contact · yenrique@msmc.com · 305-674-2625
    • Mike Cusnir · Principal investigator
    Recruiting
  • Bay Pines VA Healthcare System
    Bay Pines, Florida 33744, United States
    • Site Public Contact · Contact · vhabayresearch@va.gov · 727-398-6661
    • Ryan J. Burri · Principal investigator
    Recruiting
  • Malcom Randall Veterans Administration Medical Center
    Gainesville, Florida 32610, United States
    • Site Public Contact · Contact · trials@cancer.ufl.edu · 352-273-8675
    • Peruvemba Sriram · Principal investigator
    Recruiting
  • University of Miami Miller School of Medicine-Sylvester Cancer Center
    Miami, Florida 33136, United States
    • Site Public Contact · Contact · 305-243-2647
    • David S. Goldberg · Principal investigator
    Recruiting
  • Gastro Health - Galloway
    Miami, Florida 33176, United States
    Recruiting
  • Mount Sinai Medical Center
    Miami Beach, Florida 33140, United States
    Recruiting
  • Sarasota Memorial Hospital-Venice
    N. Venice, Florida 34275, United States
    • Site Public Contact · Contact · 941-261-9000
    • Kenneth L. Meredith · Principal investigator
    Recruiting
  • First Physicians Group - Gastroenterology Obesity Medicine
    Sarasota, Florida 34239, United States
    • Site Public Contact · Contact · 941-262-0410
    • Kenneth L. Meredith · Principal investigator
    Recruiting
  • FPG - Surgical Oncology Clinics Gastrointestinal Oncology Surgery
    Sarasota, Florida 34239, United States
    Recruiting
  • Sarasota Memorial Hospital
    Sarasota, Florida 34239, United States
    • Site Public Contact · Contact · 941-917-2225
    • Kenneth L. Meredith · Principal investigator
    Recruiting
  • Sarasota Memorial Health Care Center at University Parkway
    Sarasota, Florida 34243, United States
    • Site Public Contact · Contact · 941-917-6519
    • Kenneth L. Meredith · Principal investigator
    Recruiting
  • Piedmont Hospital
    Atlanta, Georgia 30309, United States
    Active, not recruiting
  • Augusta University Medical Center
    Augusta, Georgia 30912, United States
    • Site Public Contact · Contact · ga_cares@augusta.edu · 706-721-2388
    • Anand P. Jillella · Principal investigator
    Recruiting

Showing the first 100 of 493 sites across 2 countries.

07

References and documents

Individual participant data

Plan to share: Yes — NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05080673
Lead sponsor
NRG Oncology
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Oct 18, 2021
Start date
Feb 9, 2022
Primary completion
Nov 1, 2035 (estimated)
Completion
Nov 1, 2065 (estimated)
Last update
Sep 2, 2026

Study contacts

Director, Department of Regulatory Affairs
Contact
langerj@nrgoncology.org
412-339-5300
Norman Wolmark, MD
Contact
Robert Schoen, MD
study chair · University of Pittsburgh

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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