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The Fecal Microbiota Transplantation Registry

The Fecal Microbiota Transplantation Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03787771
Enrollment
3000
Registered
2018-12-26
Start date
2017-07-02
Completion date
2046-11-30
Last updated
2024-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Bowel Diseases

Keywords

Fecal Microbiota Transplantation

Brief summary

The human intestinal microbiota is composed of complex community of 10\*13 to 10\*14 commensal microorganisms\[1\]. Human intestine provides a nutrient-rich habitat for intestinal microorganism which allows a diverse ecosystem to enhance their host's immune system and facilitate digestive activities. Numerous researches are investigating the role of gut microbiota in human homeostasis, which may be related to the pathogenesis of gastrointestinal disease and autoimmune disorder. Fecal microbiota transplantation (FMT) is defined as infusion of feces from healthy donors to affected subjects. FMT works by altering the patient's microbiome and it is now recommended as an effective therapy for Clostridium difficile infection (CDI) not responding to standard therapies\[8\]. It has attracted great interest in recent years and many researches are exploring the FMT's potential role for treating other gastrointestinal disease such as IBD. A FMT registry is required to explore the relationship between disease prognosis and intestinal microbiota.

Detailed description

The human intestinal microbiota is composed of complex community of 10\*13 to 10\*14 commensal microorganisms\[1\]. Human intestine provides a nutrient-rich habitat for intestinal microorganism which allows a diverse ecosystem to enhance their host's immune system and facilitate digestive activities. Numerous researches are investigating the role of gut microbiota in human homeostasis, which may be related to the pathogenesis of gastrointestinal disease and autoimmune disorder. A research using gene-sequencing technique showed an abnormal microbiota composition such as specific group of Escherichia coli and decreased diversity of intestinal microbiota in individuals with Inflammatory Bowel Disease (IBD) \[2-4\]. These microbiotas may stimulate the production of cytokine and chemokines that leads to the mucosal inflammatory activity\[5\]. Gut microbiota may also link with the development of obesity and diabetes by affecting host fat storage and increasing energy harvest from the diet\[6-7\]. Fecal microbiota transplantation (FMT) is defined as infusion of feces from healthy donors to affected subjects. FMT works by altering the patient's microbiome and it is now recommended as an effective therapy for Clostridium difficile infection (CDI) not responding to standard therapies8. It has attracted great interest in recent years and many researches are exploring the FMT's potential role for treating other gastrointestinal disease such as IBD. A recent clinical study evaluated the efficacy of FMT in active Ulcerative Colitis. It showed one-forth cases of the FMT group were in UC remission and an increase in diversity of microbiota composition. However, these results were dependent on the donor\[9\]. There will be increasing use of FMT in clinical practice, as well as more studies investigating the effectiveness of FMT on other diseases in the future. However, as an emerging procedure, there is currently no registry system to track patient safety information of FMT. It is also equally important to promote scientific investigation around gut microbiome. Therefore, the investigators aim to establish a FMT registry platform to collect clinical data and specimen from FMT recipients and donors. This registry is initiated Hong Kong, and will be expanded to other part of Asia.

Interventions

None listed

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age ≥ 18 * Written informed consent obtained * Subject who has received or planning to receive FMT or other gut-related microbiota products in routine clinical practice or research (FMT recipents) * Subject who has donated stool or planning to donate stool for FMT or production of other gut-related microbiota products in routine clinical practice or research. Subjects who failed screening will also be recruited. (FMT donors)

Exclusion criteria

* Age ≤18

Design outcomes

Primary

MeasureTime frameDescription
Set up a FMT registry10 yearsSet up a registry of FMT to collect data such as demographics, past medical history, surgery, severity of disease indicated for FMT cases

Secondary

MeasureTime frameDescription
Factors associated with successful FMT10 yearsStudy samples will collected to characterize which microbiota favors FMT by performing metagenomics of gut microbiome in stool samples
Characterize FMT stool donors and other gut-related microbiota products10 yearsCollect study samples to characterize which microbiota favors FMT by metagenomics
FMT in Asia10 yearsGather information such as the severity of disease, any adverse event related to FMT and hospitalization from other study sites in Asia. Survey
Patient outcome of FMT10 yearsCompare the severity of disease, any adverse event related to FMT and hospitalization between baseline and FMT. Survey
Future research studies10 yearsNumber of patients who may be eligible for participation in future research studies by collecting their information demographics, past medical history, surgery, severity of disease
Developing Biobank of FMT10 yearsCollect and store of study samples from recipients and donors to characterize which microbiota favors FMT by metagenomics
Promoting scientific investigation in FMT10 yearsCollect study samples to characterize which microbiota favors FMT by metagenomics

Countries

Hong Kong

Contacts

Primary ContactSiew Chien Ng, PhD
siewchienng@cuhk.edu.hk852-35053996

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026