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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04294615
Other study ID # LL-KY-20150305
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2016
Est. completion date March 31, 2018

Study information

Verified date March 2020
Source Fourth Military Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to evaluate the clinical efficacy and safety of fecal microbiota transplantation by automatic methods in the treatment of moderate to severe active ulcerative colitis. There are two groups according to FMT pathway ( through a naso-jejunal tube or transendoscopic enteral tubing). Patients were followed up until 2 weeks after the final FMT in hospital.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date March 31, 2018
Est. primary completion date March 16, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Eligible patients required a diagnosis of ulcerative colitis made by a primary gastroenterologist based upon history, physical exam, laboratory/radiological studies and gastrointestinal histology. All patients were age = 18 year old at the time of enrollment. They had moderate to severe symptoms with a mayo score between 6~12 and an endoscopic subscore =2. Patient medication for UC could not have changed for at least one month prior to FMT.

Exclusion Criteria:

- Active or history of intraabdominal abscess, acute abdomen or other clinical emergencies requiring emergent management, pregnancy, prior history of FMT, prior history of TNF inhibitors use, or other serious systemic disease.

Study Design


Intervention

Other:
FMT through a naso-jejunal tube
Prepared feces by automatic methods, then the purified fecal microbiota was delivered into the intestine through a naso-jejunal tube.
FMT through TET
Prepared feces by automatic methods, then the purified fecal microbiota was delivered into the intestine through a transendoscopic enteral tubing (TET) which is fixed to the cecum with clips under endoscopic guidance.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fourth Military Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary clinical response reduction in the Mayo score of =3 points and =30% from baseline, with a decrease in the rectal bleeding subscore of =1 point or a subscore of =1 2 weeks after FMT
Secondary clinical remission, safety and progression of disease clinical remission: Mayo score = 2, with no subscore > 1; progression of disease: measured by initiation of anti-TNFa or colectomy. Adverse event severity and relatedness was graded using NIH criteria. 2 weeks after FMT
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