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A Pilot Study Examining Low Sulfur Diet as Treatment for Persistent Symptoms in Quiescent Crohn's Disease

Primary Purpose

Crohn's Disease in Remission

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low Sulfur Diet
Usual Diet
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn's Disease in Remission focused on measuring Crohn's disease, Quiescent Crohn's disease, Low sulfur diet, Microbiome

Eligibility Criteria

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

Inclusion Criteria: Prior diagnosis of Crohn's disease based on endoscopic, radiographic, and/or histologic findings Quiescent Crohn's disease as defined by fecal calprotectin level less than 150 micrograms/gram (mcg/g) stool and/or absence of inflammation on colonoscopy within 30 and 90 days, respectively, of enrollment Persistent symptoms will be defined by abdominal pain and diarrhea T-scores greater than or equal to 60 by the National Institutes of Health (NIH) Patient-Reported outcomes measurement information system Gastrointestinal scale (PROMIS-GI) Exclusion Criteria: Prior total colectomy Presence of an end ileostomy or colostomy in place Changes in immunosuppressive medications within the past 4 weeks Use of antibiotics or probiotics within the past 4 weeks Habitual vegetarian or vegan diet Active or suspected gastrointestinal stricture or stenosis Unable or unwilling to follow a low sulfur diet Currently pregnant or breastfeeding

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Low Sulfur Diet

Usual Diet

Arm Description

Participants in this group will follow a low sulfur diet. This diet decreases the amount of animal products (including meat, dairy, and eggs) as well as sulfur additives in the diet. The main types of foods in the low sulfur diet include fruits, vegetables, whole grains, nuts, seeds, and soy products.

Participants in this group will follow a standard of care usual diet for 8 weeks.

Outcomes

Primary Outcome Measures

Dietary Protein Intake for both groups as assessed by 24 hour diet recall
Dietary protein intake (animal-based) as assessed by 24 hour diet recall
Dietary Protein Intake as assessed by 24 hour diet recall
Dietary protein intake (animal-based) as assessed by 24 hour diet recall. This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.
Change in 24 hour urinary sulfate
Change in 24 hour urinary sulfate level from baseline
Change in 24 hour urinary sulfate
Change in 24 hour urinary sulfate level from baseline. This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed

Secondary Outcome Measures

Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500).
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500). This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500).
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500). This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.

Full Information

First Posted
April 25, 2023
Last Updated
July 22, 2023
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT05849012
Brief Title
A Pilot Study Examining Low Sulfur Diet as Treatment for Persistent Symptoms in Quiescent Crohn's Disease
Official Title
A Pilot Study Examining Low Sulfur Diet as Treatment for Persistent Symptoms in Quiescent Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2023 (Anticipated)
Primary Completion Date
May 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

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

5. Study Description

Brief Summary
The goal of this study is to learn about a low sulfur diet in patients with Crohn's disease. Study participants will be randomized to receive a low sulfur diet or usual diet for 8 weeks. Participants will work with study nutritionists and receive dietary educational materials. Participants will attend 2 in-person visits as well as 6 phone visits during the study. In addition, subjects will undergo testing, including a test to measure rectal sensation, a test to look for small intestinal bacterial overgrowth, and a test to measure leaky gut.
Detailed Description
Even in the absence of active inflammation, persistent symptoms are reported in up to 46% of inflammatory bowel disease (IBD) patients, especially in Crohn's disease (CD). While persistent symptoms in quiescent Crohn's disease result in worsened quality of life and worse outcomes, evidence-based treatments do not currently exist due to lack of mechanistic understanding of this condition. The gut microbiome, which are the microbes that live in our gut, have been suggested as a potential cause of persistent symptoms. Diet is a major influence on the microbiome and may have a modifiable impact on persistent symptoms in Crohn's disease. However, this has not been well established. The investigators propose a study period of approximately 8 weeks to evaluate the effects of a low sulfur diet in Crohn's disease. Participants will have an initial phone visit to determine eligibility to participate in the study and to review potential participants normal diet with a study nutritionist. The treatment phase of 8 weeks will begin at the baseline visit (week 0). Participants will be randomized to receive a low sulfur diet or usual diet for 8 weeks. Participants on the low sulfur diet will meet with the study nutritionist to receive educational materials and recipes for the low sulfur diet. During this visit, participants will undergo testing, including a rectal barostat test to evaluate rectal sensation, glucose hydrogen breath test to assess for small intestinal bacterial overgrowth, lactulose-mannitol test to evaluate intestinal permeability, and a 24-hour urine sample to measure urine sulfate levels. Participants will be asked to collect saliva, serum, and stool samples. Participants will then have phone visits every 2 weeks (week 2, week, 4, and week 6). Study nutritionists will monitor their dietary history and answer questions about the low sulfur diet if applicable. At the conclusion of the 8 weeks, participants will have a final in-person study visit where rectal barostat, glucose hydrogen breath test, lactulose mannitol testing, and 24-hour urine sulfate level will be repeated. Stool and serum samples will be collected by participants. Optional Low Sulfur Diet for participants randomized to the usual diet: At the conclusion of the study (week 8), if participants randomized to usual diet are interested, will be offered treatment with a low sulfur diet for the next 8 weeks. Participants will meet with the study nutritionist that will provide educational materials on a low sulfur diet. Participants will have phone visits every 2 weeks (week 10, week 12, and week 14) to review dietary history and answer questions about the low sulfur diet. At the conclusion of the 16 weeks, participants will have a final in-person study visit where they will undergo testing, including a rectal barostat test to evaluate rectal sensation, glucose hydrogen breath test to assess for small intestinal bacterial overgrowth, lactulose-mannitol test to evaluate intestinal permeability, and a 24-hour urine sample to measure urine sulfate levels. Participants will be asked to collect saliva, serum, and stool samples.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease in Remission
Keywords
Crohn's disease, Quiescent Crohn's disease, Low sulfur diet, Microbiome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
20 subjects will be randomized to receive either a low sulfur diet or usual diet.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low Sulfur Diet
Arm Type
Experimental
Arm Description
Participants in this group will follow a low sulfur diet. This diet decreases the amount of animal products (including meat, dairy, and eggs) as well as sulfur additives in the diet. The main types of foods in the low sulfur diet include fruits, vegetables, whole grains, nuts, seeds, and soy products.
Arm Title
Usual Diet
Arm Type
Active Comparator
Arm Description
Participants in this group will follow a standard of care usual diet for 8 weeks.
Intervention Type
Other
Intervention Name(s)
Low Sulfur Diet
Intervention Description
Subjects will be placed on a low sulfur diet for 8 weeks with the support of a nutritionist. In addition, participants will be asked to complete: surveys, lactulose-mannitol test, glucose hydrogen breath test, blood samples, visceral sensation test, 24-hour urine sample for sulfate level, provide stool samples, optional colonoscopy.
Intervention Type
Other
Intervention Name(s)
Usual Diet
Intervention Description
Subjects will continue on their usual diet for 8 weeks. At the end of 8 weeks, if participants are interested, they will be offered treatment with low sulfur diet for 8 weeks with the support of a nutritionist. In addition, participants will be asked to complete: surveys, lactulose-mannitol test, glucose hydrogen breath test, blood samples, visceral sensation test, 24-hour urine sample for sulfate level, provide stool samples, optional colonoscopy.
Primary Outcome Measure Information:
Title
Dietary Protein Intake for both groups as assessed by 24 hour diet recall
Description
Dietary protein intake (animal-based) as assessed by 24 hour diet recall
Time Frame
8 weeks
Title
Dietary Protein Intake as assessed by 24 hour diet recall
Description
Dietary protein intake (animal-based) as assessed by 24 hour diet recall. This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.
Time Frame
Approximately 16 weeks
Title
Change in 24 hour urinary sulfate
Description
Change in 24 hour urinary sulfate level from baseline
Time Frame
8 weeks
Title
Change in 24 hour urinary sulfate
Description
Change in 24 hour urinary sulfate level from baseline. This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed
Time Frame
Approximately 16 weeks
Secondary Outcome Measure Information:
Title
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
Description
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500).
Time Frame
Week 4
Title
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
Description
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500). This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.
Time Frame
Approximately week 12
Title
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
Description
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500).
Time Frame
Week 8
Title
Tolerability of Low Sulfur Diet based on the Visual Analog Scale (VAS)
Description
The VAS has 5 questions in which participants are asked about knowledge, purchase, preparation, ease of following the diet, and overall tolerability of the sulfur diet. Each question participants will score between 0-100 (higher score is more tolerable with total points of 500). This is for the group that voluntarily goes on the low sulfur diet after standard of care arm is completed.
Time Frame
Approximately 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prior diagnosis of Crohn's disease based on endoscopic, radiographic, and/or histologic findings Quiescent Crohn's disease as defined by fecal calprotectin level less than 150 micrograms/gram (mcg/g) stool and/or absence of inflammation on colonoscopy within 30 and 90 days, respectively, of enrollment Persistent symptoms will be defined by abdominal pain and diarrhea T-scores greater than or equal to 60 by the National Institutes of Health (NIH) Patient-Reported outcomes measurement information system Gastrointestinal scale (PROMIS-GI) Exclusion Criteria: Prior total colectomy Presence of an end ileostomy or colostomy in place Changes in immunosuppressive medications within the past 4 weeks Use of antibiotics or probiotics within the past 4 weeks Habitual vegetarian or vegan diet Active or suspected gastrointestinal stricture or stenosis Unable or unwilling to follow a low sulfur diet Currently pregnant or breastfeeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Allen Lee, MD, MS
Phone
734-936-9454
Email
allenlee@umich.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Queen Saunyama
Email
saunayma@med.umich.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Allen Lee, MD, MS
Organizational Affiliation
Assistant Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Allen Lee, MD, MS
Phone
734-936-9454
Email
allenlee@umich.edu
First Name & Middle Initial & Last Name & Degree
Allen Lee, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
To be determined

Learn more about this trial

A Pilot Study Examining Low Sulfur Diet as Treatment for Persistent Symptoms in Quiescent Crohn's Disease

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