RECRUITING

A Trial of Omeprazole and Low Dose Aspirin to Identify Colorectal Biomarkers of Preventive Efficacy

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This trial will obtain biomarker data on the possible preventive effects of omeprazole and low-dose aspirin in colorectal tissue. Persons who have had 5 or more adenomas, 5 or more serrated polyps, or an incompletely removed adenoma or serrated polyp in the colon or rectum are potentially eligible. Before participating in the study, study staff will explain the study and review the consent form. If you are interested and provide consent, study staff will then confirm your eligibility. Once enrolled, participants will take two 20 mg omeprazole tablets and two 81 mg aspirin tablets each day before the first meal each day for 25-45 days. The study does involve biopsies of the colorectal tissue before and after taking the study medications. The biopsies are samples of tissue, about the size of a grain of rice, that will be taken from the colon or rectum before and after taking the study medications. This is done during a usual, clinical colonoscopy exam and during one more limited exam, called flexible sigmoidoscopy, that is done for the research study. The flexible sigmoidoscopy requires less preparation. Which procedure comes first depends on what fits best with each participant's clinical scenario. Biopsies of both normal mucosa and polyps (if possible) are collected.

Official Title

An Early Phase 1 Trial of Omeprazole and Low Dose Aspirin to Identify Colorectal Biomarkers of Preventive Efficacy: The Omeprazole and Aspirin Polyp Prevention Study

Quick Facts

Study Start:2024-06-14

Study Completion:2026-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06378398

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 75 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Age 18-75 * Individuals who are due for a standard of care colonoscopy. * Have a prior history of colorectal neoplasia including any ONE of the following: * Multiple (\>=5) colorectal adenomas on most recent colonoscopy * Multiple (\>=5) sessile serrated polyps on most recent colonoscopy * Serrated polyps meeting criteria for serrated polyposis syndrome * History of incompletely resected colorectal polyp(s) (adenoma or sessile serrated polyp) on most recent colonoscopy * Willing to avoid taking non-steroidal anti-inflammatory drugs that are not provided by the study in the 30 days prior to Visit 1 and while on study. * Willing to avoid taking proton pump inhibitors that are not provided by the study in the 30 days prior to Visit 1 and while on study. * Women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) for the duration of study participation since endoscopy is not recommended during pregnancy. * Demonstrate adequate organ and marrow function obtained within the last 60 days as defined below: * Absolute neutrophil count ≥1,000/microliter * Platelets ≥100,000/microliter * Total bilirubin ≤ 1.5 fold of the institutional upper limit of normal Note: Higher total bilirubin levels (≤ 3 mg/dL) can be allowed if due to known benign liver condition such as Gilbert's * AST (SGOT)/ALT (SGPT) ≤3.0 fold of the institutional upper limit of normal * Creatinine ≤1.5 fold of the institutional upper limit of normal * Patients on chronic suppressive antiviral therapy for herpes simplex virus (HSV) are eligible. * Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial. * For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated. * Ability to understand and the willingness to sign a written informed consent document.	* Age 76 or higher since there is an increased risk of GI bleeding and peptic ulcer disease in persons above 75 years of age. * Pathogenic germline variants in adenomatous polyposis coli (APC) and DNA mismatch repair (MMR) genes associated with Lynch Syndrome, or biallelic pathogenic germline variants in the MutY homologue glycosylase (MUTYH) gene. * Have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to proton pump inhibitors and/or aspirin. * Participants may not be receiving any other investigational agents. * Have a history of prior aspirin or NSAID gastritis with bleeding. * Currently taking a proton pump inhibitor and unable/unwilling to discontinue use 30 days prior to Visit 1. * Taking NSAIDs or aspirin \>25% of the time (\>8 days/month) and unable/unwilling to discontinue use 30 days prior to Visit 1 and until Visit 4. * Currently taking medications associated with increased risk for bleeding (warfarin, Eliquis, Plavix, etc.). * Currently taking medications that have interactions with omeprazole: atazanavir, erlotinib, levoketoconazole, nelfinavir, pazopanib, rilpivirine, sparsentan, certain azole antifungals (itraconazole, ketoconazole, and posaconazole). * Have a history of hemophilia, Von Willebrand disease or any other known bleeding diathesis. * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. * Individuals who the site physician investigator assesses as at high risk for bleeding due to heavy alcohol use or comorbid conditions. * Pregnant women are excluded since endoscopy is not recommended while pregnant. * Have invasive cancer or being treated for invasive cancer at the current time or within the past 36 months, with the exception of cancers curatively removed by surgery, other than melanoma, and stage I and II cervical squamous cell cancers.

Inclusion Criteria

Exclusion Criteria

* Age 18-75
* Individuals who are due for a standard of care colonoscopy.
* Have a prior history of colorectal neoplasia including any ONE of the following:
* Multiple (\>=5) colorectal adenomas on most recent colonoscopy
* Multiple (\>=5) sessile serrated polyps on most recent colonoscopy
* Serrated polyps meeting criteria for serrated polyposis syndrome
* History of incompletely resected colorectal polyp(s) (adenoma or sessile serrated polyp) on most recent colonoscopy
* Willing to avoid taking non-steroidal anti-inflammatory drugs that are not provided by the study in the 30 days prior to Visit 1 and while on study.
* Willing to avoid taking proton pump inhibitors that are not provided by the study in the 30 days prior to Visit 1 and while on study.
* Women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) for the duration of study participation since endoscopy is not recommended during pregnancy.
* Demonstrate adequate organ and marrow function obtained within the last 60 days as defined below:
* Absolute neutrophil count ≥1,000/microliter
* Platelets ≥100,000/microliter
* Total bilirubin ≤ 1.5 fold of the institutional upper limit of normal Note: Higher total bilirubin levels (≤ 3 mg/dL) can be allowed if due to known benign liver condition such as Gilbert's
* AST (SGOT)/ALT (SGPT) ≤3.0 fold of the institutional upper limit of normal
* Creatinine ≤1.5 fold of the institutional upper limit of normal
* Patients on chronic suppressive antiviral therapy for herpes simplex virus (HSV) are eligible.
* Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.
* For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
* Ability to understand and the willingness to sign a written informed consent document.

* Age 76 or higher since there is an increased risk of GI bleeding and peptic ulcer disease in persons above 75 years of age.
* Pathogenic germline variants in adenomatous polyposis coli (APC) and DNA mismatch repair (MMR) genes associated with Lynch Syndrome, or biallelic pathogenic germline variants in the MutY homologue glycosylase (MUTYH) gene.
* Have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to proton pump inhibitors and/or aspirin.
* Participants may not be receiving any other investigational agents.
* Have a history of prior aspirin or NSAID gastritis with bleeding.
* Currently taking a proton pump inhibitor and unable/unwilling to discontinue use 30 days prior to Visit 1.
* Taking NSAIDs or aspirin \>25% of the time (\>8 days/month) and unable/unwilling to discontinue use 30 days prior to Visit 1 and until Visit 4.
* Currently taking medications associated with increased risk for bleeding (warfarin, Eliquis, Plavix, etc.).
* Currently taking medications that have interactions with omeprazole: atazanavir, erlotinib, levoketoconazole, nelfinavir, pazopanib, rilpivirine, sparsentan, certain azole antifungals (itraconazole, ketoconazole, and posaconazole).
* Have a history of hemophilia, Von Willebrand disease or any other known bleeding diathesis.
* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
* Individuals who the site physician investigator assesses as at high risk for bleeding due to heavy alcohol use or comorbid conditions.
* Pregnant women are excluded since endoscopy is not recommended while pregnant.
* Have invasive cancer or being treated for invasive cancer at the current time or within the past 36 months, with the exception of cancers curatively removed by surgery, other than melanoma, and stage I and II cervical squamous cell cancers.

Contacts and Locations

Study Contact

Kirsten Tuck

CONTACT

734-763-1141

KLtuck@med.umich.edu

Principal Investigator

Zora Djuric

PRINCIPAL_INVESTIGATOR

University of Michigan Rogel Cancer Center

Study Locations (Sites)

The University of Michigan Rogel Cancer Center

Ann Arbor, Michigan, 48109

United States

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, 43210

United States

Collaborators and Investigators

Sponsor: University of Michigan Rogel Cancer Center

Zora Djuric, PRINCIPAL_INVESTIGATOR, University of Michigan Rogel Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-14

Study Completion Date2026-01

Study Record Updates

Study Start Date2024-06-14

Study Completion Date2026-01

Terms related to this study

Additional Relevant MeSH Terms

Colorectal Neoplasia