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Standardized Fecal Microbiota Transplantation for Inflammatory Bowel Disease (SFMT-IBD)

Y

Yanling Wei

Status and phase

Unknown
Phase 2

Conditions

Inflammatory Bowel Disease
Ulcerative Colitis
Crohn's Disease

Treatments

Drug: Mesalazine
Procedure: FMT

Study type

Interventional

Funder types

Other

Identifiers

NCT02335281
TMMU-DP-GI-FMT-001

Details and patient eligibility

About

There are many limitations in the current treatments of Inflammatory bowel disease (IBD). Now the investigators realized that the intestinal microecological is closely associated with the development of IBD. So the standardized fecal microbiota transplantation is considered to be simple but effective emerging therapies for the treatment of IBD. In this project the investigators intend to carry out a single-center, randomized, single-blind clinical intervention study. The investigators will recruit 40 patients with IBD (20 cases of Ulcerative Colitis and 20 cases of Crohn's disease) in China. The patients will be randomly divided into 2 groups, one group will be given treatment of standardized fecal microbiota transplantation, the other will be simply treated with mesalazine, followed up for at least 1 year. The investigators propose to determine the efficiency, durability and safety of Standardized Fecal Microbiota Transplantation for IBD treatment.

Full description

In this projects the investigators aim to re-establish a gut balance of intestinal microecological through Standardized Fecal Microbiota Transplantation for IBD (UC and CD). We will establish a standardized isolation, store, and transportion steps of fecal bacteria from donated fresh stool in the laboratory. Then the bacteria will be transplanted to mid-gut by nose-jejunum nutrition tube. Patients in this study will be assigned to receive standardized FMT only once or traditional medicine of mesalazine and would be followed up for at least 1 year. The clinical symptoms, sign, blood tests, abdominal CT, endoscopy and questionnaire will be used to assess the efficiency, durability and safety of Standardized FMT at the start and end of the projects.

Enrollment

40 estimated patients

Sex

All

Ages

16 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Severe IBD define as HBI score ≥ 9.
  • Moderate IBD define as 7<HBI <9
  • Montreal classification: Age > 14 years old, Location L1-3, Behavior B1-3.

Exclusion criteria

  • Diarrhea activity scores < 3
  • Severely active disease with perianal diseases
  • Severely active disease with indication of surgery.
  • Diagnosis as IBD first time or first year.
  • No history of using 5-ASA, biological (antibody), immunomodulatory therapy, corticosteroid therapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Standardized FMT
Experimental group
Description:
The group include 20 patients. They will receive standardized FMT. The FMT was given to mid-gut by nose-jejunum nutrition tube. It was given only once.
Treatment:
Procedure: FMT
Mesalazine
Active Comparator group
Description:
This group include 20 patients . The patients will receive traditional medicine of mesalazine treatment.
Treatment:
Drug: Mesalazine

Trial contacts and locations

1

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Central trial contact

Dongfeng Chen, doctor; Yanling Wei, doctor

Data sourced from clinicaltrials.gov

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