search
Back to results

The Effect of Intestinal Microbiota Transplantation for Inflammatory Bowel Diseases (IBD)

Primary Purpose

Inflammatory Bowel Disease(IBD)

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Intestinal Microbiota Transplantation
Sponsored by
Zhongshan Hospital Xiamen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Disease(IBD) focused on measuring Inflammatory Bowel Disease(IBD), Ulcerative colitis(UC), Crohn's disease(CD), intestinal microbiota transplantation, microbiota

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Standard or conventional medicine treatment ineffective of Inflammatory Bowel Diseases(IBD) patients
  • IBD patients with recurrent symptoms
  • IBD patients who had drug dependence or recurrence when reduced or discontinued use
  • Untreated IBD patients who voluntarily received Standardized Intestinal Microbiota Transplantation(IMT)
  • Written informed consent/assent as appropriate

Exclusion Criteria:

  • IBD patients with contraindications for gastrointestinal endoscopy
  • IBD patients with indication of surgery
  • Moderate and severe renal injuty(serum creatinine>2mg/dL or 177mmol/L), moderate and severe chronic obstructive pulmonary disease, severe hypertension, cerebrovascular accident, congestive heart failure, unstable angina pectoris
  • Other serious diseases that may interfere the recruitment or affect the survival, such as cancer or acquired immune deficiency syndrome
  • Mentally or legally disabled person
  • Preparing for pregnancy
  • Medical or social condition which in the opinion of the principal investigator would interfere with or prevent regular follow up
  • Participating in other clinical trials.

Sites / Locations

  • Zhongshan Hospital Affiliated to Xiamen UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Standardized IMT

traditional drugs

Arm Description

The patients will receive Standardized Intestinal Microbiota Transplantation(Standardized IMT). The IMT was given to mid-gut by nose-jejunum nutrition tube or capsules. It was given three times a week.

The patients will receive traditional medicine treatment as usual.

Outcomes

Primary Outcome Measures

The change of the modified Mayo score
Clinical remission defined as modified Mayo score≦2. Change from baseline will be assessed at different timepoint.The endpoint of follow-up is the time of clinical recurrence.

Secondary Outcome Measures

The change of CDAI
Clinical remission defined as CDAI(Crohn's disease activity index )≦150.Change from baseline will be assessed at different timepoint. The endpoint of follow-up is the time of clinical recurrence.
Relief of gastrointestinal symptoms
The onset and duration of gastrointestinal symptoms will be assessed by "Evaluation Score Table of Gastrointestinal Symptoms".Change from baseline will be assessed at different timepoint.
Changes of gut microbiota
Alpha and Beta diversity of GI microbiota by High-throughput sequencing on baseline line and1 month, 3 months, 6months ,12 months after treatment.

Full Information

First Posted
October 27, 2017
Last Updated
May 24, 2021
Sponsor
Zhongshan Hospital Xiamen University
search

1. Study Identification

Unique Protocol Identification Number
NCT03426683
Brief Title
The Effect of Intestinal Microbiota Transplantation for Inflammatory Bowel Diseases
Acronym
IBD
Official Title
Efficacy, Safety and Microbiota of Intestinal Microbiota Transplantation for Inflammatory Bowel Diseases
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 21, 2017 (Actual)
Primary Completion Date
October 2021 (Anticipated)
Study Completion Date
November 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhongshan Hospital Xiamen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There are many limitations in the current treatments of Inflammatory Bowel Diseases(IBD) which includes Ulcerative Colitis(UC) and Crohn's Disease(CD). Some patients have no or little reaction to the traditional drugs. Now the investigators realized that the intestinal microbiota is closely associated with the development of Inflammatory Bowel Diseases. In recent years, a retrospective study showed that the overall efficiency of intestinal microbiota transplantation for IBD was 79%, the overall remission rate was 43%, which opened a new chapter in the treatment of IBD. So the standardized intestinal 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 plan to recruit patients with IBD in China. The patients will be randomly divided into two groups, one group will be given treatment of standardized intestinal microbiota transplantation, the other will be simply treated with traditional drugs, followed up for at least 1 year. The investigators aim to determine the efficiency, durability and safety of Intestinal Microbiota Transplantation for IBD treatment, and further to explore which major bacteria may effect in this project.
Detailed Description
In this projects the investigators aim to re-establish a gut balance of intestinal microbiota through Standardized Intestinal Microbiota Transplantation for Ulcerative Colitis(UC) and Crohn's Disease(CD).Investigators have established a standardized isolation, store, and transport 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 or capsules.Participants in this study will be assigned to receive Standardized Intestinal Microbiota Transplantation three times a week or traditional medicine and would be followed up for at least 1 year. The clinical symptoms, sign, blood tests, endoscopy and questionnaire will be used to assess the efficiency, durability and safety of Standardized Intestinal Microbiota Transplantation at the start and end of the projects. At last, investigators will use 16S-rDNA to estimate the change of intestinal microbiota.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease(IBD)
Keywords
Inflammatory Bowel Disease(IBD), Ulcerative colitis(UC), Crohn's disease(CD), intestinal microbiota transplantation, microbiota

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
an open label, parallel study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standardized IMT
Arm Type
Experimental
Arm Description
The patients will receive Standardized Intestinal Microbiota Transplantation(Standardized IMT). The IMT was given to mid-gut by nose-jejunum nutrition tube or capsules. It was given three times a week.
Arm Title
traditional drugs
Arm Type
No Intervention
Arm Description
The patients will receive traditional medicine treatment as usual.
Intervention Type
Other
Intervention Name(s)
Intestinal Microbiota Transplantation
Intervention Description
the bacteria will be transplanted to mid-gut by nose-jejunum nutrition tube. Patients in this study will be assigned to receive standardized IMT three times or traditional medicine and would be followed up for at least 3 year.
Primary Outcome Measure Information:
Title
The change of the modified Mayo score
Description
Clinical remission defined as modified Mayo score≦2. Change from baseline will be assessed at different timepoint.The endpoint of follow-up is the time of clinical recurrence.
Time Frame
1 month, 3 months, 6months, 12 months
Secondary Outcome Measure Information:
Title
The change of CDAI
Description
Clinical remission defined as CDAI(Crohn's disease activity index )≦150.Change from baseline will be assessed at different timepoint. The endpoint of follow-up is the time of clinical recurrence.
Time Frame
1 month, 3 months, 6months,12 months
Title
Relief of gastrointestinal symptoms
Description
The onset and duration of gastrointestinal symptoms will be assessed by "Evaluation Score Table of Gastrointestinal Symptoms".Change from baseline will be assessed at different timepoint.
Time Frame
1 months, 3 months, 6 months, 12months
Title
Changes of gut microbiota
Description
Alpha and Beta diversity of GI microbiota by High-throughput sequencing on baseline line and1 month, 3 months, 6months ,12 months after treatment.
Time Frame
1 months, 3 months, 6 months, 12months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Standard or conventional medicine treatment ineffective of Inflammatory Bowel Diseases(IBD) patients IBD patients with recurrent symptoms IBD patients who had drug dependence or recurrence when reduced or discontinued use Untreated IBD patients who voluntarily received Standardized Intestinal Microbiota Transplantation(IMT) Written informed consent/assent as appropriate Exclusion Criteria: IBD patients with contraindications for gastrointestinal endoscopy IBD patients with indication of surgery Moderate and severe renal injuty(serum creatinine>2mg/dL or 177mmol/L), moderate and severe chronic obstructive pulmonary disease, severe hypertension, cerebrovascular accident, congestive heart failure, unstable angina pectoris Other serious diseases that may interfere the recruitment or affect the survival, such as cancer or acquired immune deficiency syndrome Mentally or legally disabled person Preparing for pregnancy Medical or social condition which in the opinion of the principal investigator would interfere with or prevent regular follow up Participating in other clinical trials.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yanyun Fan
Phone
18759212670
Email
trudy1@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Qiongyun Chen
Phone
18850311573
Email
709136659@qq.com
Facility Information:
Facility Name
Zhongshan Hospital Affiliated to Xiamen University
City
Xiamen
State/Province
Fujian
ZIP/Postal Code
361000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanyun Fan
Phone
18759212670
Email
trudy1@163.com
First Name & Middle Initial & Last Name & Degree
Qiongyun Chen
Phone
18850311573
Email
709136659@qq.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

The Effect of Intestinal Microbiota Transplantation for Inflammatory Bowel Diseases

We'll reach out to this number within 24 hrs