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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: JPRN
Last refreshed on: 17 October 2023
Main ID:  JPRN-UMIN000018642
Date of registration: 11/08/2015
Prospective Registration: Yes
Primary sponsor: Juntendo university school of medicine Department of gastroenterology
Public title: A trial of fecal microbiota transplantation and / or antibiotics therapy for ulcerative colitis
Scientific title: A trial of fecal microbiota transplantation and / or antibiotics therapy for ulcerative colitis - A trial of fecal microbiota transplantation and / or antibiotics therapy for ulcerative colitis
Date of first enrolment: 2015/08/12
Target sample size: 50
Recruitment status: Complete: follow-up complete
URL:  https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021579
Study type:  Interventional
Study design:  Parallel Non-randomized  
Phase:  Not selected
Countries of recruitment
Japan
Contacts
Name:     Dai Ishikawa
Address:  2-1-1Hongo, Bunkyoku Tokyo Japan
Telephone: 03-3813-3111
Email: dai@juntendo.ac.jp
Affiliation:  Juntendo university school of medicine Department of gastroenterology
Name:     Dai Ishikawa
Address:  2-1-1Hongo, Bunkyoku Tokyo Japan
Telephone: 03-3813-3111
Email: dai@juntendo.ac.jp
Affiliation:  Juntendo university school of medicine Department of gastroenterology
Key inclusion & exclusion criteria
Inclusion criteria:
Exclusion criteria: 1. Patients who have severe drug allergy are excluded. 2. Donors who show abnormal findings to the screening tests including blood and feces.

Age minimum: 6years-old
Age maximum: Not applicable
Gender: Male and Female
Health Condition(s) or Problem(s) studied
ulcerative colitis
Intervention(s)
Antibiotics therapy:Taking three kinds of antibiotics (Amoxicillin, fosmycin, metronidazole) for two weeks.
FMT:Administration of the fecal material from healthy donors to patients.
Primary Outcome(s)
Efficacy of this treatment is evaluted by microbiota analysis, endoscopic score and bllod test.
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Juntendo university school of medicine Department of gastroenterology
Secondary Sponsor(s)
Ethics review
Status: YES
Approval date: 31/07/2015
Contact:
Results
Results available: Yes
Date Posted:
Date Completed: 31/08/2016
URL:
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