Infection With Multi-drug Resistant Organisms Clinical Trial
Official title:
Use of Fecal Microbiota Transplantation (FMT) to Reverse Multi-Drug Resistant Organism Carriage
| NCT number | NCT02312986 |
| Other study ID # | 201506131 |
| Secondary ID | |
| Status | Completed |
| Phase | Phase 1 |
| First received | |
| Last updated | |
| Start date | August 2015 |
| Est. completion date | July 31, 2020 |
| Verified date | February 2021 |
| Source | Washington University School of Medicine |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This proposed protocol involves the use of the fecal microbiota transplantation (FMT) to suppress or reverse colonization with multidrug resistant organisms (MDRO) in subjects with recurrent MDRO infections due to organisms of likely enteric origin. FMT will be performed on subjects with a history of at least three recurrent infections due to MDRO; at least two recurrent, severe infections due to MDRO requiring hospitalization; or at least two recurrent infections due to MDRO for which only antimicrobials with rate limiting toxicities are available. The objective of this protocol is to determine if fecal microbiota transplantation (FMT) will be able to prevent additional recurrences of infections due to MDRO by suppressing or reversing enteric colonization with MDRO.
| Status | Completed |
| Enrollment | 1 |
| Est. completion date | July 31, 2020 |
| Est. primary completion date | July 31, 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion criteria will include: - Age =18 years old. - Outpatient status at time of FMT. - History of at least three recurrent infections due to an MDRO; at least two recurrent, severe infections due to MDRO requiring hospitalization; or at least two recurrent infections due to MDRO for which only antimicrobials with rate limiting toxicities (see above) are available AND the MDRO is likely of enteric origin. Only MDROs of likely enteric origin will be included. - Be without active infection due to the MDRO at the time of FMT. - Not be receiving antimicrobials (therapeutic or suppressive) within 48 hours of FMT. Exclusion criteria will include: - Subjects <18 years old. - Subjects unable to be seen as an outpatient. - Use of enteral or systemic antimicrobials at time of FMT. - Planned use of enteral or systemic antimicrobials up to 6 months post-FMT. - Pregnancy or inability/unwillingness to use contraceptives. - Recent intra-abdominal surgery - Short gut syndrome - Gastrointestinal motility disorders - Use of medications that affect intestinal motility an inability to cease using those medications at the time of FMT. - Post-allogeneic hematopoietic stem cell transplant recipients with previous or current gastrointestinal graft versus host disease. - ANC <500/mm3 - HIV+ and not well controlled on antiretroviral therapy, or CD4+ <200/ mm3 - At increased risk for peritonitis: presence of intra-abdominal devices, receiving peritoneal dialysis, or ascites. - Any acute illness - Recurrent C. difficile infection. - Unlikely to survive for 3 months. - Investigator feels the risks of FMT outweigh potential benefit, including other conditions or medications that the investigator determines puts the subject at greater risk from FMT. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Washington University School of Medicine |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Safety of FMT in Patients With Recurrent MDRO Infections (Incidence and Severity of Solicited and Serious Adverse Events) | Incidence and severity of solicited and serious adverse events within 12 months of FMT. | 12 months post-FMT | |
| Secondary | MDRO Infection Status Post-FMT (Number of Subjects With MDRO Infections) | Number of subjects with MDRO infections 30 days, 6 months, and 12 months post-FMT. | 30 days, 6 months, and 12 months post-FMT |