The Effect of Fecal Microbiota Transplantation on the Decolonization of Multidrug-resistant Organisms

NCT ID: NCT04583098

Last Updated: 2025-06-19

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-03-14
• Study Completion Date: 2024-08-31

Brief Summary

The purpose of this study is to assess the effect of fecal microbiota transplantation for the decolonization of carbapenem-resistant Enterobacteriaceae or vancomycin-resistant Enterococci in the gut.

Detailed Description

This study is a prospective observational cohort study exploring the decolonization effect of Fecal Microbiota Transplantation (FMT) in patients colonized with Carbapenem-resistant Enterobacteriaceae (CRE) and Vancomycin-resistant Enterococci (VRE).

Patients who have provided written consent for participation in the study will be required to maintain fasting starting from the evening before the procedure, after discontinuing broad-spectrum antibiotics for a minimum of 3-7 days. Subsequently, a bowel preparation will be carried out twice - the evening before and the morning of the procedure. Once the bowel preparation is complete, 1 hour before the procedure, patients will receive loperamide to reduce bowel movements and then proceed to the endoscopy suite.

Fecal microbiota transplantation (FMT) will be carried out with the acquired frozen donor stool, which will be thawed for 2 hours at room temperature following purchase and delivery from a stool bank, under the consent and supervision of the patient or guardian. Frozen stool from carefully screened donors who have passed the rigorous screening of both Stage 1 clinical assessment and Stage 2 laboratory tests (including evaluation for antibiotic resistance organisms) will be supplied from a stool bank of Microbiotix inc. (Hyun Soo Seo, et al. Ann Lab Med 2021;41:424-428).

The FMT procedure will be conducted in collaboration with the research team in the Division of Gastroenterology. During the procedure, no tissue biopsy or excessive endoscope insertion will be performed. The FMT involves the simple infusion of thawed donor stool into the terminal ileum under colonoscopy, which takes approximately 5-10 minutes. The procedure carries minimal risk of bleeding, perforation, or aspiration. In most cases, it will be performed under sedation with colonoscopy. If smooth insertion of the colonoscope or proper visualization of the colon is hindered, or if colonic preparation is not successful, Esophagogastroduodenoscopy (EGD) will be performed with sedation, and thawed donor stool will be infused into the third portion of the duodenum. This procedure also poses minimal risk of regurgitation or aspiration due to its anatomical and physiological characteristics. After the procedure, the lower extremities will be elevated by about 30 degrees to prevent the transplanted stool from exiting. A one-day fasting period will be maintained after the procedure to facilitate successful engraftment of the transplanted stool, followed by the gradual resumption of a regular diet. Following FMT, repeated rectal swab cultures will be conducted to confirm three consecutive negative results for CP-CRE or VRE at 3-7 day intervals.

In cases where encapsulated fecal material is used for FMT, it will be ingested along with high-acid cranberry or orange juice. The capsules are specially designed to dissolve in low-acidic environments, allowing them to reach the terminal ileum for safe administration without the need for bowel preparation. On the first day, 15 capsules will be consumed, followed by another 15 capsules on the second day, for a total of 30 capsules. Subsequently, repeated rectal swab tests will be conducted to confirm three consecutive negative results for CP-CRE or VRE at 3-day intervals.

According to patient random allocation, fecal samples and clinical metadata will be periodically collected (prior to FMT, 1 month, 3 months, 6 months, and 12 months after FMT) from both recipients and donors. These collected samples will undergo full-length 16S rRNA sequencing and shotgun metagenomic sequencing to comprehensively analyze the gut microbiome. Through this analysis, the aim is to elucidate the intestinal microorganisms associated with decolonization outcomes and mechanisms.

Conditions

Carbapenem-Resistant Enterobacteriaceae Infection; Vancomycin-Resistant Enterococcal Infection

Study Design

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

Study Groups

carbapenem-resistant Enterobacteriaceae

FMT using frozen or capsulized stool

fecal microbiota transplantation

Intervention Type: OTHER

frozen or capsulized stool from donors who had already finished recommended blood \& stool screening for stool donors

vancomycin-resistant Enterococci

FMT using frozen or capsulized stool

fecal microbiota transplantation

Intervention Type: OTHER

frozen or capsulized stool from donors who had already finished recommended blood \& stool screening for stool donors

Interventions

fecal microbiota transplantation

frozen or capsulized stool from donors who had already finished recommended blood \& stool screening for stool donors

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients over 19 years-old with carbapenem-resistant Enterobacteriaceae(CRE) or vancomycin-resistant Enterococci(VRE) rectal colonization
• Patients who have received written informed consent for fecal microbiota transplantation and collection of stool samples

Exclusion Criteria

• Patients who have not completed acute-phase treatment, including antibiotic treatment
• If patients are pregnant, may be pregnant, or are lactating
• Patients who have not received written informed consent for the study enrollment
• Patients who are judged to be unhelpful to participate in the study according to the researcher's judgment

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Chuncheon Sacred Heart Hospital

OTHER

Sponsor Role: lead

Responsible Party

Seung Soon Lee

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Seung Soon Lee, MD

Role: PRINCIPAL_INVESTIGATOR

Chuncheon Sacred Heart Hospital

Locations

Chuncheon Sacred Heart Hospital

Chuncheon, Gangwon-do, South Korea

Countries

South Korea

Other Identifiers

2020-08-006

Identifier Type: -

Identifier Source: org_study_id