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Use of a Novel Diet (UC DIET) for Treatment of Mild to Moderate Active Pediatric Ulcerative Colitis

Primary Purpose

Ulcerative Colitis (UC)

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Ulcerative Colitis Diet
Antibiotic cocktail
Sponsored by
Prof. Arie Levine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis (UC)

Eligibility Criteria

8 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Informed consent
  2. Established diagnosis of UC.
  3. Age: 8 - 19 years ( inclusive)
  4. Mild to moderate active disease, 10 ≤ PUCAI ≤45.
  5. Stable medication (IMM/ 5ASA) use for the past 6 weeks. Patients who have received topical 5ASA therapy for <7 days and are active may be included if topical therapy is stopped at enrolment

Exclusion Criteria:

Exclusion criteria:

  1. Any proven current infection such as positive stool culture, parasite or C. difficile.
  2. Antibiotic or Steroids use in the past 2 weeks.
  3. PUCAI >45
  4. Acute severe UC in the previous 12 months.
  5. Current Extra intestinal manifestation of UC.
  6. PSC or Liver disease
  7. Pregnancy.
  8. Allergy to one of the antibiotics or age <11 will exclude patients from entering the antibiotic arm

Sites / Locations

  • The Children's Hospital of Philadelphia
  • IWK Health Centre, Dalhousie University
  • The E. Wolfson.Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Ulcerative Colitis Diet

Antibiotic Treatment

Arm Description

Patients will receive a structured novel diet termed the UCD for 6 weeks, and those in remission at week 6 will receive the step down diet for another 6 weeks.

This antibiotic treatment will be given as an open label for patients who refuse diet therapy or for patients who show no improvement by week 3 , deteriorate by week 6, or patients who are not in full remission by week 6 will receive a 14 day course of antibiotics as previously described by Kato and colleagues.

Outcomes

Primary Outcome Measures

Remission rate, defined as a PUCAI less than 10 at week 6.

Secondary Outcome Measures

Mean PUCAI week 6
Mean Calprotectin at week 6
Physicians Global Assessment week 6
Remission week 12, defined as a PUCAI less than 10
Mean PUCAI week 12

Full Information

First Posted
January 19, 2015
Last Updated
May 29, 2022
Sponsor
Prof. Arie Levine
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1. Study Identification

Unique Protocol Identification Number
NCT02345733
Brief Title
Use of a Novel Diet (UC DIET) for Treatment of Mild to Moderate Active Pediatric Ulcerative Colitis
Official Title
Use of a Novel Diet (UC DIET) Targeting the Microbiota for Treatment of Mild to Moderate Active Pediatric Ulcerative Colitis: An Open Label Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2015 (Actual)
Primary Completion Date
October 29, 2021 (Actual)
Study Completion Date
October 29, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Arie Levine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of the study is to evaluate strategies that target the microbiota for the treatment of Ulcerative Colitis , This study will involve a novel diet that the investigators developed , based on the hypothesis that UC involves dysbiosis , underutilzation of certain metabolic pathways and use of pathways that increase risk of inflammation . The investigators have postulated that manipulation of colonic bacterial metabolism with this diet will induce remission in UC without involving additional immune suppression.
Detailed Description
Ulcerative colitis is a chronic inflammatory disease primarily involving the colon. It has long been considered to be due to a dysregulated immune response targeting the colon, and involves unknown environmental factors . Recent studies have highlighted several characteristics which may suggest that UC is associated with alterations of the microbiota, defective production of short chain fatty acids and an impaired mucous layer. However at present, no effective therapy targets the microbiota or its interaction with the colonic epithelium. UC in humans is characterized by increased mucosal sulfides and increased sulfate and sulfide reducing bacteria and activation of amino acid metabolism pathways which impair butyrate production, whereas certain dietary patterns in humans and rodent models may induce dysbiosis and favor sulphide reducing bacteria. Further support for targeting the microbiota includes several studies demonstrating that antibiotics might be helpful for severe refractory colitis. Development of treatment strategies that target the microbiota could reduce exposure to immune suppression, and add new therapeutic strategies that do not exist at present. Though diet has a significant impact on the composition of the microbiota no dietary intervention to date has proven effective for induction of remission. The investigators hypothesized that ulcerative colitis is caused by a series of events involving dysbiosis with sulfate or sulfide reducing bacteria combined with defective production of short chain fatty acids, coupled with a defective mucous layer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis (UC)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ulcerative Colitis Diet
Arm Type
Experimental
Arm Description
Patients will receive a structured novel diet termed the UCD for 6 weeks, and those in remission at week 6 will receive the step down diet for another 6 weeks.
Arm Title
Antibiotic Treatment
Arm Type
Experimental
Arm Description
This antibiotic treatment will be given as an open label for patients who refuse diet therapy or for patients who show no improvement by week 3 , deteriorate by week 6, or patients who are not in full remission by week 6 will receive a 14 day course of antibiotics as previously described by Kato and colleagues.
Intervention Type
Other
Intervention Name(s)
Ulcerative Colitis Diet
Intervention Description
we have postulated that a diet that we developed that reduces exposure to dietary ingredients that allow sulfide reducing bacteria to thrive, or that impair the mucous layer, coupled with dietary products that enhance butyrate production, could induce remission in UC without involving additional immune suppression.
Intervention Type
Drug
Intervention Name(s)
Antibiotic cocktail
Other Intervention Name(s)
•Doxycyclin, amoxicillin and metronidazole
Intervention Description
We have postulating that antibiotic therapy can alter the microbiota clinically. Controlling the microbiota by antibiotics may allow for control of the disease without immune suppression
Primary Outcome Measure Information:
Title
Remission rate, defined as a PUCAI less than 10 at week 6.
Time Frame
week 6
Secondary Outcome Measure Information:
Title
Mean PUCAI week 6
Time Frame
week 6
Title
Mean Calprotectin at week 6
Time Frame
week 6
Title
Physicians Global Assessment week 6
Time Frame
week 6
Title
Remission week 12, defined as a PUCAI less than 10
Time Frame
week 12
Title
Mean PUCAI week 12
Time Frame
week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent Established diagnosis of UC. Age: 8 - 19 years ( inclusive) Mild to moderate active disease, 10 ≤ PUCAI ≤45. Stable medication (IMM/ 5ASA) use for the past 6 weeks. Patients who have received topical 5ASA therapy for <7 days and are active may be included if topical therapy is stopped at enrolment Exclusion Criteria: Exclusion criteria: Any proven current infection such as positive stool culture, parasite or C. difficile. Antibiotic or Steroids use in the past 2 weeks. PUCAI >45 Acute severe UC in the previous 12 months. Current Extra intestinal manifestation of UC. PSC or Liver disease Pregnancy. Allergy to one of the antibiotics or age <11 will exclude patients from entering the antibiotic arm
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arie Levine, MD
Organizational Affiliation
Wolfson Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
IWK Health Centre, Dalhousie University
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
9700
Country
Canada
Facility Name
The E. Wolfson.Medical Center
City
Holon
ZIP/Postal Code
58100
Country
Israel

12. IPD Sharing Statement

Learn more about this trial

Use of a Novel Diet (UC DIET) for Treatment of Mild to Moderate Active Pediatric Ulcerative Colitis

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