Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05373784
Other study ID # STUDY00000055
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date March 15, 2024
Est. completion date May 30, 2025

Study information

Verified date March 2024
Source University of Massachusetts, Worcester
Contact Justin A Maykel, MD
Phone 508-334-8195
Email justin.maykel@umassmemorial.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Fecal Microbiota Transplantation (FMT) is an established treatment for Clostridium difficile (C. diff) infection refractory to medical management. As C. diff infection usually arises due to significant disturbances in the gut microbiome, FMT is typically performed to restore a healthy microbiome among affected patients who have failed other treatments. Diverticulitis is a major, and often recurrent, source of morbidity in the U.S for which antibiotics and surgical resection constitute the only treatment options to date. Although alterations of the intestinal microbiome have also been shown among patients with diverticular disease, research on FMT in diverticulitis is sparse. The intended goal of this project is to determine the feasibility, effectiveness and safety of FMT in the treatment of uncomplicated diverticulitis, using clinical outcomes and microbiome analyses.


Description:

This study aims to assess the safety and efficacy of fecal microbiota transplantation (FMT) in treating uncomplicated diverticulitis. FMT will be delivered via colonoscopy using donor stool. Fecal material samples obtained from the University of Minnesota Microbiota Therapeutics Program (UMMTP) will be used each patients FMT. These samples undergo FDA mandated testing prior to being used as donor samples. Recipients will undergo FMT via Colonoscopy at UMASS Memorial Medical Center and will be monitored for one hour after the procedure to ensure they are not experiencing any adverse events. They will receive a phone call 24 hours and 2 weeks after their procedure to ensure that they are at their baseline health. Recipients follow-up visits will occur at one month, 3 month, 6 months and 1 year post FMT. Baseline stool samples will be collected from both the recipients and the UMMTP samples for baseline metagenomic sequencing. Recipient stool samples will be obtained weekly for the first month, then at 3 months, 6 months and 1 year. Microbiome analyses will also performed on recipient all stool samples post FMT to assess for successful engraftment of donor's microbiota onto the recipient's.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date May 30, 2025
Est. primary completion date March 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Recipient Inclusion Criteria: 1. Age >18 2. One or more prior episode(s) of uncomplicated diverticulitis, as confirmed by imaging and clinical symptoms. 3. Eligible for surgical resection Recipient Exclusion Criteria: 1. Subjects <18 years of age 2. Patients with active diverticulitis flare 3. Evidence of complicated diverticulitis (diverticulitis with abscess/phlegmon, bleeding, stricture, fistula or perforation) on imaging 4. Prior fecal transplant 5. Patients unable to provide informed consent 6. Pregnant and/or breastfeeding women 7. Prisoners 8. Students 9. Prior small or large bowel obstruction within the past year 10. Prior major gastrointestinal or intra-abdominal surgery 11. Any major illness or condition that may substantially increase risks to the recipient based on the investigator's judgment. 12. Sexually active women who adhere to natural family planning alone Donor Inclusion Criteria: 1. Adult patients =18 years old 2. Colonoscopy screening as recommended by the American Cancer Society. However, it is to be noted that only recipients will undergo colonoscopy for receipt of FMT as part of the study, not donors. We will only ensure that the prospective donor follows the recommended guidelines for screening colonoscopy, which are to begin at the age of 45. If the donor does not meet such guidelines, s/he will not be allowed to proceed as a donor. If a donor is not yet eligible to undergo screening colonoscopy (i.e., younger than 45), this will not be required of him/her." 3. Able to provide informed consent Donor Exclusion Criteria: 1. History of diverticulitis 2. Recent COVID-19 infection, confirmed or suspected exposure to COVD-19 within the past eight weeks. Such subjects will be excluded irrespective of negative COVID nasopharyngeal test. 3. Risk of infectious agent - Known exposure to HIV, syphilis, or viral hepatitis (within the previous 12 months) - High-risk sexual behaviors including sexual contact with anyone with HIV/AIDS or hepatitis, men who have sex with men, sex for drugs or money - Use of illicit intravenous (IV) drug use - Tattoo or body piercing within 6 months - Incarceration within previous 12 months - Known current communicable disease (e.g., COVID 19, Influenza, STDs, HIV/AIDS, Hepatitis B and C) - Risk factors for variant Creutzfeldt-Jacob disease to prevent potential transmission of abnormal/pathologic prions (cellular proteins), which are the basis of this disease. - Receipt of blood transfusion from country other than the United States of America (USA) and Canada in the previous 6 months 4. Individuals who are at a higher risk for colonization with multi-drug resistant organisms (MDRO): - Health care workers - Persons who have been hospitalized or discharged from long-term care facilities in the past 30 days - Persons who regularly attend outpatient medical or surgical clinics - Persons who have engaged in medical tourism in the past 30 days 5. Gastrointestinal comorbidities - History of inflammatory bowel disease - History of celiac disease - History of irritable bowel syndrome, idiopathic chronic constipation, or chronic diarrhea - History of gastrointestinal malignancy 6. Other - Antibiotic use within the preceding 90 days - Ingestion of a potential allergen (e.g., nuts) where recipient has a known allergy to this agent within the past 30 days - Systemic autoimmunity (e.g., multiple sclerosis, connective tissue disease) - Chronic pain syndromes (e.g., chronic fatigue syndrome, fibromyalgia) - Fever, defined as temperature of 100 F or 38.7C, on the day of stool donation. Potential donors will be allowed to re-screen within 1 week if febrile on the day of stool donation. . - Sexually active women who adhere to natural family planning alone as method of contraception - Prisoners - Students - Pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Fecal Microbiota Transplantation (FMT)
Fecal microbiota transplantation (FMT) involves administering fecal material from a healthy individual into the gastrointestinal tract of another individual. This is currently an accepted method of treatment for recurrent colitis secondary to Clostridium difficile infection refractory to antibiotics/medical management. FMT can be delivered via capsule endoscopy or via colonoscopy. In this study, it will be administered via colonoscopy.

Locations

Country Name City State
United States UMASS Memorial Medical Center Worcester Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Justin Maykel

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of diverticular flares/attacks since FMT After FMT, recipients/participants will be asked to report the number of diverticulitis episodes they have experienced since FMT 1 year
Primary Number of emergency room visits and hospitalizations due to diverticulitis since FMT After FMT, recipients/participants will be asked to report the number of times (if any) they presented to the emergency room or were hospitalized due to diverticulitis. 1 year
Primary Number of courses of antibiotics required for the treatment of diverticulitis since FMT After FMT, recipients/participants will be asked to report whether they required any antibiotics due to diverticulitis 1 year
Primary Necessity for surgery After FMT, recipients/participants will be asked to report whether they required surgery to treat diverticulitis 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT03042091 - Neomycin and Metronidazole Hydrochloride With or Without Polyethylene Glycol in Reducing Infection in Patients Undergoing Elective Colorectal Surgery Early Phase 1
Completed NCT02246361 - Impact of Six Patient Information Leaflets (PIL) on Doctor Patient Communication Phase 4
Completed NCT01476995 - Prognostic Indicators as Provided by the EPIC ClearView N/A
Completed NCT01081054 - Hospitalization or Ambulatory Treatment of Acute Diverticulitis Phase 4
Completed NCT00195351 - Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection Phase 4
Completed NCT03337984 - Damage Control Surgery in the Treatment of Complicated Diverticulitis
Recruiting NCT06210724 - FIT in Diverticulitis
Completed NCT01986686 - Recurrence Following Nonoperative Management of 1st Episode of Hinchey II Diverticulitis N/A
Completed NCT01477190 - Spinal Analgesia for Colonic Resection Using an Enhanced Recovery After Surgery (ERAS) Program Phase 1/Phase 2
Completed NCT01056913 - NITI CAR27 (ColonRing) Compression Anastomosis in Colorectal Surgery Phase 4
Completed NCT00468455 - Post-Op Quality of Life After Colorectal Surgery N/A
Completed NCT00230971 - Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection (cIAI) Phase 4
Enrolling by invitation NCT03700593 - Feasibility and Safety of Single Port Robot in Colorectal Procedures
Recruiting NCT04095663 - Comparison of Surgery and Medicine on the Impact of Diverticulitis (COSMID) Trial N/A
Completed NCT00545740 - Prevention of Recurrence of Diverticulitis Phase 3
Recruiting NCT01837342 - Multicenter Study Comparing Morbidity and Quality of Life Associated in the Treatment by Surgical Resection and the Conservative Treatment, After Favorable Evolution of Purulent Peritonitis That Originates From Diverticulitis Treated by Mini-invasive Surgery N/A
Completed NCT01727388 - Informativeness to Digital Rectal Examination Phase 3
Completed NCT00554099 - Asacol Acute Diverticulitis(DIVA)Study Phase 2
Completed NCT04173182 - Confocal Laser Endomicrospy in Colonic Diverticular Disease
Completed NCT02200055 - Using Electrical Bioimpedance Assessments to Estimate Perioperative Total Body Water and Postoperative Fluid Need N/A