The AGA Fecal Microbiota Transplantation (FMT) National Registry will assess short- and long-term patient outcomes associated with FMT. This registry is a program of the AGA Institute and AGA Center for Gut Microbiome Research & Education.
If you perform fecal microbiota transplantation (FMT), we encourage you to participate in this national data collection project. Our goal is to track 4,000 patients for 10 years. The data we collect will allow us to identify potential short-term adverse outcomes and to search for long-term safety concerns, such as development of chronic conditions like irritable bowel syndrome, obesity and diabetes. Please contribute to advancing the future of FMT — the information available to you and your patients at the end of this initiative will be worth it.
With this milestone, the FMT registry is officially underway. The AGA FMT National Registry also announces collaborations with American Gut and OpenBiome.
Genome Magazine profiles AGA’s Fecal Microbiota Transplantation National Registry, which will be the largest data set of long-term outcomes for this procedure.
AGA’s Fecal Microbiota Transplantation National Registry: an important step toward understanding risks and benefits of microbiota therapeutics
In this Gastroenterology commentary, the registry co-principal investigators discuss the impetus and goals for this massive data collection initiative.
Read our initial announcement of the AGA FMT National Registry.
Visit Clinicaltrials.gov to see the sites participating in this registry. You or your doctor can contact the participating sites to learn more about enrolling.
Visit this page for frequently asked questions and other information relevant to patients who have already received a FMT.
This information will help you understand if fecal microbiota transplantation is right for you.
Watch this brief video to hear as leading experts in the field explain what are fecal transplants and how they’ve changed the treatment of recurring C. difficile infection.
More on the AGA FMT National Registry
Hear from Loren Laine, MD, AGAF, Colleen Kelly, MD, and Gary Wu, MD, co-principal investigators for AGA’s NIH-funded FMT registry, as they explain how this registry will influence future practice and research of FMT.
Meet our funder
The content on this website is solely the responsibility of the American Gastroenterological Association and does not necessarily represent the official views of the National Institutes of Health.
Meet our steering committee
The FMT Registry Steering Committee oversees registry operations, ensures compliance with clinical protocol and applicable regulations, and provides general direction for the registry.
Colleen Kelly, MD, Co-Chair and Prinicipal Investigator, Brown University Women’s Medicine and Collaborative
Loren Laine, MD, AGAF, Co-Chair and Co-Principal Investigator, Yale School of Medicine
Gary Wu, MD, Co-Principal Investigator, University of Pennsylvania
Ashish Atreja, MD, Health Information Technology Expert, Mount Sinai Hospital
Stacy Kahn, MD, NASPGHAN Liaison, Boston Children’s Hospital
James Lewis, MD, MSCE, AGAF, Clinical Epidemiology Expert, University of Pennsylvania
Thomas Moore, MD, IDSA Liaison, Infectious Disease Consultants of Kansas
David Rubin, MD, AGAF, CCFA Liaison, University of Chicago
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