Fecal Microbiota Transplant National Registry

This registry will prospectively enroll 4,000 patients who undergo FMT at 75 sites throughout
North America. Information on FMT methodology employed (e.g., screening of donor and
recipient, preparation, FMT delivery) will be collected from each site. The indication for
FMT as well as baseline information on recipient will also be collected. Following FMT,
patients will be followed at regular intervals up to 10 years post FMT. This will include
follow-up information from the patient's healthcare provider at 1 month, 6 months, 1 year,
and 2 years after FMT as well as direct communication with patients at least annually up to
10 years after FMT. Follow-up information collected will be designed to assess potential
short-term and long-term safety and effectiveness.

Inclusion Criteria:

- Recipient Inclusion Criteria

- Ability to give informed consent

- Receiving FMT or other gut-related microbiota product within 90 days after
providing consent

- Access to internet and/or telephone

- Donor Inclusion

- Ability to give informed consent

- Providing stool sample for FMT

Exclusion Criteria:

- Incarceration