Fecal Microbiota Transplant National Registry
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Feb 7, 2024
Trial Information
Current as of July 01, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
The Fecal Microbiota Transplant National Registry is a clinical trial that aims to collect important information about the safety and effectiveness of fecal microbiota transplantation (FMT) and other related gut treatments. FMT involves transferring healthy bacteria from a donor’s stool to help improve gut health in patients who may be suffering from certain conditions. This study will gather data from medical records and phone calls to better understand how these treatments work over time. Please note that this study will not include newborns.
To participate, individuals must be able to provide informed consent and be planning to receive FMT or a similar gut treatment within 90 days of agreeing to join the study. Participants will also need access to the internet or a phone. Donors, who provide stool samples for FMT, must also meet similar consent criteria. It’s important to mention that people who are currently incarcerated cannot participate in this trial. Overall, participants can expect to contribute to valuable research that could help improve future treatments for gut health.
Gender
ALL
Eligibility 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 Criteria:
- • Ability to give informed consent
- • Providing stool sample for FMT
- Exclusion Criteria:
- • Incarceration
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Trial Officials
Max Brondfield, MD
Principal Investigator
University of California, San Francisco
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported