Study of Inflammatory Markers and Symptom Severity in Personalized Nutritional Intervention in IBS
Primary Purpose
IBS - Irritable Bowel Syndrome, Inflammation
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Rotation Diet
Sponsored by

About this trial
This is an interventional treatment trial for IBS - Irritable Bowel Syndrome
Eligibility Criteria
Inclusion Criteria:
- IBS (according to ROME IV criteria)
- blood analysis within 1yr with CBC, TSHr, ESR, CRP, urine, glucose
- attitude to change dietary habits
- willing to follow study protocol
Exclusion Criteria:
- low BMI (<18.5 kg/m2)
- pregnancy
- restrictive dietary habits (e.g. veganism)
- positive FOBT
- faecal calprotectin >200 mcg/g
- known or recurrent bowel infections
- known or recurrent UTI (>3/yr)
- former diverticulitis
- alcohol abuse
- major concurrent disease (e.g. IBD, coeliac disease, eating disorder,...)
- pharmacological treatment with drugs that alter intestinal motility (e.g. PPI, metformin,...)
Sites / Locations
- GEK srl
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Intervention
Arm Description
Subjects were then instructed to avoid the foods highlighted in their personal food profile in certain days of the week, and to assume them in 7 of the 21 meals of the week
Outcomes
Primary Outcome Measures
BAFF levels
reduction of BAFF levels from baseline
PAF levels
reduction of PAF levels from baseline
Secondary Outcome Measures
IBS symptom severity
IBS symptom severity score reduction from baseline
BMI
BMI reduction from baseline
Full Information
NCT ID
NCT04348760
First Posted
April 14, 2020
Last Updated
April 15, 2020
Sponsor
GEK Srl
Collaborators
Hippocrates Research
1. Study Identification
Unique Protocol Identification Number
NCT04348760
Brief Title
Study of Inflammatory Markers and Symptom Severity in Personalized Nutritional Intervention in IBS
Official Title
Study of Two Inflammatory Cytokines, BAFF and PAF, and Their Clinical Relevance Before and After a Personalized Nutritional Intervention in IBS Subjects
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
July 30, 2019 (Actual)
Study Completion Date
July 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GEK Srl
Collaborators
Hippocrates Research
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
Irritable Bowel Syndrome (IBS) is a widespread disease with variable symptoms that have an important impact on the quality of life. Despite the prevalence of IBS, its etiology and pathophysiology are still to be fully understood, but immune response is known to be involved. In this study, the investigators researched the variation of two specific cytokines, B-cell activating factor (BAFF) and platelet-activating factor (PAF), the levels of food-specific IgG and the symptom severity, using Irritable Bowel Syndrome - Symptom Severity Score (IBS-SSS), following a personalized an unrestricted-calorie diet.
Detailed Description
The investigators enrolled 30 subjects with diagnosis of IBS, according to Rome-IV criteria, whose inflammatory markers were measured at baseline and after 6 weeks of dietary intervention. The subjects were monitored in a general practice outpatient setting (GP) and nutritional advice was offered remotely via two telephone sessions with a nutritionist. The researchers investigated the variation of two specific cytokines, B-cell activating factor (BAFF) and platelet-activating factor (PAF), the levels of food-specific IgG and the symptom severity, using Irritable Bowel Syndrome - Symptom Severity Score (IBS-SSS).
Data monitoring was ensured by an external monitor (Hippocrates Research, Genova, Italy).
All data entry was in accordance with GCP protocol, and AE were classified using CTCAE 4.0
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
IBS - Irritable Bowel Syndrome, Inflammation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Subjects were then instructed to avoid the foods highlighted in their personal food profile in certain days of the week, and to assume them in 7 of the 21 meals of the week
Intervention Type
Behavioral
Intervention Name(s)
Rotation Diet
Intervention Description
Based on the food-specific IgG measurement and relative distribution, a personalized food profile was created for each subject identifying 1 to 3 relevant food groups/nutritional clusters. Subjects were then instructed to avoid the foods highlighted in their personal food profile in certain days of the week, and to assume them in 7 of the 21 meals of the week. No calorie restriction was imposed in the diet.
Primary Outcome Measure Information:
Title
BAFF levels
Description
reduction of BAFF levels from baseline
Time Frame
6 weeks
Title
PAF levels
Description
reduction of PAF levels from baseline
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
IBS symptom severity
Description
IBS symptom severity score reduction from baseline
Time Frame
6 weeks
Title
BMI
Description
BMI reduction from baseline
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
IBS (according to ROME IV criteria)
blood analysis within 1yr with CBC, TSHr, ESR, CRP, urine, glucose
attitude to change dietary habits
willing to follow study protocol
Exclusion Criteria:
low BMI (<18.5 kg/m2)
pregnancy
restrictive dietary habits (e.g. veganism)
positive FOBT
faecal calprotectin >200 mcg/g
known or recurrent bowel infections
known or recurrent UTI (>3/yr)
former diverticulitis
alcohol abuse
major concurrent disease (e.g. IBD, coeliac disease, eating disorder,...)
pharmacological treatment with drugs that alter intestinal motility (e.g. PPI, metformin,...)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emiliana Tognon, PhD
Organizational Affiliation
GEK Srl
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mattia Cappelletti, MD
Organizational Affiliation
SMA srl
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Attilio F Speciani, MD
Organizational Affiliation
GEK Srl
Official's Role
Study Director
Facility Information:
Facility Name
GEK srl
City
Milano
ZIP/Postal Code
20149
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participants data that underline the results reported in article, after deidentification (text, tables)
IPD Sharing Time Frame
immediately following and for 36 months after publication
IPD Sharing Access Criteria
Proposals should be directed to the PI/Sponsor. To gain access, data requestors will need to sign a data access agreement
Citations:
PubMed Identifier
30288077
Citation
Ng QX, Soh AYS, Loke W, Lim DY, Yeo WS. The role of inflammation in irritable bowel syndrome (IBS). J Inflamm Res. 2018 Sep 21;11:345-349. doi: 10.2147/JIR.S174982. eCollection 2018.
Results Reference
background
PubMed Identifier
20353497
Citation
Lied GA, Lillestol K, Valeur J, Berstad A. Intestinal B cell-activating factor: an indicator of non-IgE-mediated hypersensitivity reactions to food? Aliment Pharmacol Ther. 2010 Jul;32(1):66-73. doi: 10.1111/j.1365-2036.2010.04314.x. Epub 2010 Mar 26.
Results Reference
background
PubMed Identifier
23170971
Citation
Ligaarden SC, Lydersen S, Farup PG. IgG and IgG4 antibodies in subjects with irritable bowel syndrome: a case control study in the general population. BMC Gastroenterol. 2012 Nov 21;12:166. doi: 10.1186/1471-230X-12-166.
Results Reference
background
PubMed Identifier
33292297
Citation
Cappelletti M, Tognon E, Vona L, Basello K, Costanzi A, Speciani MC, Speciani AF. Food-specific serum IgG and symptom reduction with a personalized, unrestricted-calorie diet of six weeks in Irritable Bowel Syndrome (IBS). Nutr Metab (Lond). 2020 Dec 1;17(1):101. doi: 10.1186/s12986-020-00528-x.
Results Reference
derived
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Study of Inflammatory Markers and Symptom Severity in Personalized Nutritional Intervention in IBS
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