Intestinal Microbiota Transplantation in Patients Undergoing Colon Resection

Phase

Condition

N/A

Treatment

IMT

Saline solution

Clinical Study ID

NCT06370884

SURG-2023-29833

Ages 18-75
All Genders

Study Summary

This is a single-center, open-label study for safety and feasibility of IMT in patients undergoing colonic surgery. After consent, individuals of the ages of 18-75 with a history of diverticulitis or sigmoid colon cancer will be enrolled to have a feeding tube placed at the time of surgery and receive IMT solution on postoperative day 2-3 (at least 48 hours following IV antibiotics) with the subsequent removal of the feeding tube. Prior to administration of IMT, recipients will be screened for inclusion/exclusion criteria, interviewed for medical history and medications, and consented. Additionally, prior to undergoing IMT, baseline blood and fecal samples will be collected. The use of a nasogastric feeding tube has specifically been chosen over colonoscopic introduction of the IMT. This is because colonoscopy introduces increased intraluminal carbon dioxide and pressure as well as mechanical stress on the colon in the setting of a newly created bowel anastomosis, which may contribute to the potential risk of anastomotic disruption. The nasogastric feeding tube will be placed while the patient is under anesthesia under direct visualization to minimize any risk of bowel perforation, albeit very low. The study will specifically utilize a 10F 43" Corpak feeding tube (Halyard Health, Alpharetta, GA). Patients will be monitored while in-patient in person. Following discharge, they will undergo follow-up either by phone, video or in-person visit, or via online survey of symptoms and chronic medical conditions potentially related to IMT, beginning on the day following discharge through post-operative day 14, and then monthly up to 6 months post- IMT to screen for SAEs and AEs. Screening for SAEs and AEs will be done using a symptom questionnaire as well as by asking patients during our interview. Fecal samples will be collected from participants on months one, three and six post-IMT to assess for changes in recipient microbiome (engraftment kinetics).

Eligibility Criteria

Inclusion

Inclusion Criteria:

Able/willing to provide informed consent
Between 18-75 years of age
Undergoing surgery for a history of diverticulitis or sigmoid colon cancer.
Able to provide fecal samples
Stated willingness to comply with all study procedures and availability for theduration of trial to follow-up by telephone, in-person, email, and/or video visitsor correspondence

Exclusion

Exclusion Criteria:

Any history of inflammatory bowel disease
Pregnancy or breastfeeding. A pregnancy test will be obtained from females of child-bearing potential on the proposed day of IMT (prior to the receipt of IMT). Patientswith a positive pregnancy test will be excluded. A negative result will be requiredfor subjects who are females of child-bearing potential to receive IMT treatment.
Life expectancy of < 6 months
Presence of ileostomy or colostomy
Known history of inflammatory bowel disease (Crohn's, Ulcerative Colitis)
Patients on immunosuppressants (calcineurin inhibitors, prednisone ≥ 20 mg/day,methotrexate, azathioprine, immunosuppressive biologics, JAK inhibitors)
Patients with neutropenia (an absolute neutrophil count < 0.5 x 109 cells/L)obtained on a complete blood count with differential at screening.
History of solid organ or bone marrow transplant.
Anticipated recurrent antibiotic use (e.g., patients with frequent urinary tractinfections or sinusitis).
History of severe anaphylactic food allergy.
History of celiac disease.
Patients receiving cancer chemotherapy, immunotherapy, or radiation.

Study Design

IMT

February 01, 2024

September 01, 2026

Connect with a study center

University of Minnesota
Minneapolis, Minnesota 55414
United States
Active - Recruiting
University of Minnesota
Minneapolis 5037649, Minnesota 5037779 55414
United States
Site Not Available

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