Collagenase Biobank Study

NCT ID: NCT07211230

Last Updated: 2025-12-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 107 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2026-02-28
• Study Completion Date: 2026-10-31

Brief Summary

The purpose of this study is to look at how bacteria present within the stool at the time of surgery and postoperatively may contribute to the development of cancer recurrence after surgery. By collecting stool and blood before and after surgery, the researchers hope to determine if certain types of bacteria, or products that the bacteria produce, promote the development of tumors after surgery. By collecting tumor tissue and growing cell lines, we hope this will help researchers better understand the behavior of these types of tumors.

Detailed Description

The purpose of this study is to collect stool, blood, and tissue samples both before and after patients undergo surgery for colon cancer. These samples will be analyzed for their bacterial composition and function, and assayed for bacterial-derived metabolites. Additionally, these samples will be tested in the laboratory for their ability to promote tumor formation in cancer cells and in animal models of surgery. Finally, patients will undergo nutritional surveys to document their current nutritional intake. Integration of the patient's nutritional intake with the data from the analyzed biospecimens will allow the researchers to determine if these bacteria and/or their metabolites are more prevalent in patients who eat certain diets. Taken together, results from this study will provide knowledge as to the mechanisms by which tumors form after surgery and potentially allow for future therapies to prevent it.

Conditions

Colorectal (Colon or Rectal) Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• English speaking.
• All genders, races, and ethnicities.
• Aged greater or equal to 18 years of age.
• Ability to understand and the willingness to sign a written informed consent form.
• Diagnosed with a colon adenocarcinoma or presumed adenocarcinoma in which surgical resection is recommended.
• Have a planned surgical resection of the colon adenocarcinoma at the University of Chicago Comprehensive Cancer Center.
• Reside within 150 miles of the University of Chicago Comprehensive Cancer Center.

Exclusion Criteria

• Stage IV colon adenocarcinoma (known metastatic disease).
• Intravenous or oral antibiotic exposure within 30 days of surgery to treat an infection.
• Prebiotic exposure within 30 days of surgery.
• History of neoadjuvant chemotherapy/radiation to treat the primary colon adenocarcinoma.
• History of chemotherapy/radiation to treat a separate malignancy within the last 6 months.
• History or current ileostomy or colostomy.
• Allergy to perioperative medications (oral neomycin/metronidazole for preoperative bowel preparation, intraoperative prophylactic intravenous cefoxitin).
• Patients who are pregnant.
• Patients with a history of inflammatory bowel disease.
• Patients with a history of bariatric surgery.
• History of eating disorders.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of California, San Diego

OTHER

Sponsor Role: collaborator

Midwestern University

OTHER

Sponsor Role: collaborator

University of Chicago

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Benjamin P Shogan

Role: PRINCIPAL_INVESTIGATOR

University of Chicago

Locations

University of Chicago

Chicago, Illinois, United States

Countries

United States

Central Contacts

Benjamin Shogan, MD

Role: CONTACT

bshogan@bsd.uchicago.edu

(773) 732-2260

Teresa Barry

Role: CONTACT

tbarry@bsd.uchicago.edu

Facility Contacts

Teresa Barry

Role: primary

tbarry@bsd.uchicago.edu

773-702-5681

Role: backup

cdixon520@bsd.uchicago.edu

Other Identifiers

IRB25-0833

Identifier Type: -

Identifier Source: org_study_id