Elemental Diet for Treatment of Inflammatory Bowel Disease in Patients With Chronic Granulomatous Disease
Primary Purpose
Chronic Granulomatous Disease, Inflammatory Bowel Disease
Status
Enrolling by invitation
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Neocate Splash
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Granulomatous Disease focused on measuring Inflammatory Bowel Disease, Crohn disease, Ulcerative Colitis, Glucocorticoids, Microbiome
Eligibility Criteria
- INCLUSION CRITERIA:
Individuals must meet all of the following criteria to be eligible for study participation:
- Aged 8 - 65 years.
- Have confirmed diagnoses of CGD, CGD-associated colitis, and IBD.
- Have a Simple Endoscopic Score for Crohn Disease (SES-CD) > 3 and/or HBI >= 5.
- Able to provide informed consent.
- Willing to allow storage of biological samples for future research.
- Willing to allow genetic testing on biological samples.
- Willing to be admitted as inpatient for up to 2 weeks to initiate the elemental diet.
EXCLUSION CRITERIA:
- History of monoclonal antibody therapy in the past 3 months.
- Pregnancy.
- Active or ongoing infection that requires antibiotics other than the participant s known prophylaxis medications.
- Any condition that, in the opinion of the investigator, contraindicates participation in this study will be excluded from study participation.
Sites / Locations
- National Institutes of Health Clinical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
Participants will be on this diet for 4 weeks. The amount per serving will be determined on the basis of the participant s weight and caloric needs, as determined by a staff dietician.
Outcomes
Primary Outcome Measures
Change in the relative abundance of proteobacteria in stool samples obtained after elemental diet.
Change in the relative abundance of proteobacteria in stool samples obtained after elemental diet.
Secondary Outcome Measures
Unexpected AEs possibly, probably, or definitely related to the elemental diet.
Ability to tolerate 4 weeks of elemental diet as measured by > 75% of caloric intake via elemental diet over the 4-week period.
Weight loss.
Initiation of antibiotics.
Changes in fecal calprotectin, ESR, and CRP.
Changes in the HBI at completion of the elemental diet and at 4 weeks after completion.
Change in alpha and beta diversity after diet
Full Information
NCT ID
NCT03983837
First Posted
June 7, 2019
Last Updated
October 11, 2023
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
1. Study Identification
Unique Protocol Identification Number
NCT03983837
Brief Title
Elemental Diet for Treatment of Inflammatory Bowel Disease in Patients With Chronic Granulomatous Disease
Official Title
Elemental Diet for Treatment of Inflammatory Bowel Disease in Patients With Chronic Granulomatous Disease
Study Type
Interventional
2. Study Status
Record Verification Date
October 10, 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
June 23, 2021 (Actual)
Primary Completion Date
March 19, 2024 (Anticipated)
Study Completion Date
March 19, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Background:
Bacteria that live inside the stomach and intestines are important for health. Chronic granulomatous disease (CGD) and inflammatory bowel disease (IBD) can make people have unhealthy bacteria. This can lead to gastrointestinal (GI) problems. Researchers want to see if people with CGD and IBD feel better when they change the bacteria in the stomach by following a special liquid diet.
Objective:
To see if an elemental diet can change the bacteria in the stomach and intestines of people with CGD and IBD. Also, to see if this helps GI symptoms.
Eligibility:
People ages 8-65 years with CGD, CGD-associated colitis, and IBD.
Design:
Participants will first be screened with:
Upper GI endoscopy and/or colonoscopy. A long, thin tube with a tiny camera at the end will be passed into the participant s body through the mouth or anus. Tissue will be collected. Participants will be sedated for the procedure. They will be sedated using a special mask or small plastic tube placed in an arm vein using a needle.
Participants will be put on the special diet for up to 4 weeks. They will stay in the hospital for the first 1-2 weeks. They will have check-ups. They will have blood, urine, and stool samples collected. They will keep a symptom diary to record how they feel and any GI symptoms.
Participants will have 2 follow-up visits. The first will be right after they finish the diet. The second will be 4 weeks later. They will have blood, urine, and stool samples collected. They will learn about re-introducing other foods into their diet.
Detailed Description
Chronic granulomatous disease (CGD) is a rare genetic immune disorder that results in recurrent and severe infections, and inflammatory dysregulation. For almost 50% of patients with CGD, this inflammation causes severe inflammatory bowel disease (IBD). However, treatment is long term and challenging as CGD-IBD is prone to relapse, and use of immune modulators must be balanced with increased risk of infectious complications. Conventional IBD (Crohn disease and ulcerative colitis) is likely caused by an inappropriate inflammatory response to intestinal microbes, which is influenced by the environment in a genetically susceptible host. While it is not yet clear if intestinal dysbiosis is a result or cause of intestinal inflammation, studies suggest that correcting intestinal dysbiosis may improve intestinal inflammation. Studies in patients with conventional IBD suggest that strict dietary restrictions can resolve symptoms of IBD and induce remission as effectively as glucocorticoids but without the side effects of those drugs. Because these diets alter the gut microbiome, they may serve as effective treatment for CGD-IBD.
In this study, we propose to treat 5 patients >= 8 years old who have CGD and IBD with 4 weeks of an elemental diet. Participants will stay as inpatients for up to 2 weeks and will return for follow-up at the end of the diet to begin tapering off and be reintroduced to normal food. The primary objective of this study is the evaluation of changes in the microbiome before and after the elemental diet. Secondary objectives are evaluations of tolerability and safety of the diet, along with changes in local and systemic markers of inflammation, and improvement of IBD symptoms as determined by reduction in Harvey-Bradshaw Index score.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Granulomatous Disease, Inflammatory Bowel Disease
Keywords
Inflammatory Bowel Disease, Crohn disease, Ulcerative Colitis, Glucocorticoids, Microbiome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Participants will be on this diet for 4 weeks. The amount per serving will be determined on the basis of the participant s weight and caloric needs, as determined by a staff dietician.
Intervention Type
Other
Intervention Name(s)
Neocate Splash
Intervention Description
Neocate Splash is a hypoallergenic, amino acid based elemental liquid diet that is taken orally.
Primary Outcome Measure Information:
Title
Change in the relative abundance of proteobacteria in stool samples obtained after elemental diet.
Description
Change in the relative abundance of proteobacteria in stool samples obtained after elemental diet.
Time Frame
Day 56
Secondary Outcome Measure Information:
Title
Unexpected AEs possibly, probably, or definitely related to the elemental diet.
Time Frame
Day 0 to 56
Title
Ability to tolerate 4 weeks of elemental diet as measured by > 75% of caloric intake via elemental diet over the 4-week period.
Time Frame
Day 0 to 27
Title
Weight loss.
Time Frame
Day 0 to 56
Title
Initiation of antibiotics.
Time Frame
Day 0 to 56
Title
Changes in fecal calprotectin, ESR, and CRP.
Time Frame
Day 56
Title
Changes in the HBI at completion of the elemental diet and at 4 weeks after completion.
Time Frame
Day 28 and 56
Title
Change in alpha and beta diversity after diet
Time Frame
Day 56
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA:
Individuals must meet all of the following criteria to be eligible for study participation:
Aged 8-65 years.
Have confirmed diagnoses of CGD, CGD-associated colitis, and IBD.
Have a Simple Endoscopic Score for Crohn Disease (SES-CD) > 3 and/or HBI >= 5.
Able to provide informed consent.
Willing to allow storage of biological samples for future research.
Willing to allow genetic testing on biological samples.
Willing to be admitted as inpatient for up to 2 weeks to initiate the elemental diet.
EXCLUSION CRITERIA:
Pregnancy.
Active or ongoing infection that requires antibiotics other than the participant s known prophylaxis medications.
Any condition that, in the opinion of the investigator, contraindicates participation in this study will be excluded from study participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christa S Zerbe, M.D.
Organizational Affiliation
National Institute of Allergy and Infectious Diseases (NIAID)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
.Human data generated in this study will be shared for future research as follows:@@@@@@ (Summation)De-identified data in an NIH-funded or approved public repository.@@@@@@ (Summation)De-identified data in another public repository. @@@@@@ (Summation)Identified data in the Biomedical Translational Research Information System (automatic for activities in the CC).@@@@@@ (Summation)De-identified or identified data with approved outside collaborators under appropriate agreements.
IPD Sharing Time Frame
Data will be shared at the time of or shortly after publication.
IPD Sharing Access Criteria
Requests for data will be reviewed and approved/disapproved by the PI.
Citations:
PubMed Identifier
18410635
Citation
Jones LB, McGrogan P, Flood TJ, Gennery AR, Morton L, Thrasher A, Goldblatt D, Parker L, Cant AJ. Special article: chronic granulomatous disease in the United Kingdom and Ireland: a comprehensive national patient-based registry. Clin Exp Immunol. 2008 May;152(2):211-8. doi: 10.1111/j.1365-2249.2008.03644.x.
Results Reference
background
PubMed Identifier
24985400
Citation
Magnani A, Brosselin P, Beaute J, de Vergnes N, Mouy R, Debre M, Suarez F, Hermine O, Lortholary O, Blanche S, Fischer A, Mahlaoui N. Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease. J Allergy Clin Immunol. 2014 Sep;134(3):655-662.e8. doi: 10.1016/j.jaci.2014.04.014. Epub 2014 Jun 27.
Results Reference
background
PubMed Identifier
19381301
Citation
van den Berg JM, van Koppen E, Ahlin A, Belohradsky BH, Bernatowska E, Corbeel L, Espanol T, Fischer A, Kurenko-Deptuch M, Mouy R, Petropoulou T, Roesler J, Seger R, Stasia MJ, Valerius NH, Weening RS, Wolach B, Roos D, Kuijpers TW. Chronic granulomatous disease: the European experience. PLoS One. 2009;4(4):e5234. doi: 10.1371/journal.pone.0005234. Epub 2009 Apr 21.
Results Reference
background
Links:
URL
https://clinicalstudies.info.nih.gov/cgi/detail.cgi?A_2019-I-0108.html
Description
NIH Clinical Center Detailed Web Page
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Elemental Diet for Treatment of Inflammatory Bowel Disease in Patients With Chronic Granulomatous Disease
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