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Gluten Sensitivity in Non-Celiac Patients (GS)

Primary Purpose

Gluten Sensitivity

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
gluten
rice starch
Sponsored by
University of Campania "Luigi Vanvitelli"
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Gluten Sensitivity focused on measuring gluten sensitivity

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients with age between 18-65 with signs/symptoms compatible with gluten-triggered disorders
  • Patients testing negative for celiac disease either by biopsy Marsh 0-1 or those who are HLA-DQ2 and DQ8 negative, as well as tTG and EMA negative
  • Patients that improved on a gluten free diet

Exclusion Criteria:

  • Subjects diagnosed with celiac disease (positive TTG and/or EMA, and histology positive with Marsh II or above);
  • Subjects diagnosed with wheat allergy
  • Subjects with Type 1 Diabetes (T1D)
  • Subjects with Inflammatory Bowel Disease (ulcerative colitis or Crohn's disease)
  • Pregnancy
  • Subjects with Helicobacter Pylori infection and other gastrointestinal infection

Sites / Locations

  • Center for Celiac Research & Treatment, Yawkey Center for Outpatients Care
  • Università Politecnica delle Marche
  • Gastroenterologia ed Endoscopia digestiva, Ospedale San Giuseppe Moscati
  • Gastroenterology, Second University of Naples
  • Internal Medicine, Policlinico di Palermo
  • Gastroenterology, University of Salerno
  • Ospedale "Casa Sollievo della Sofferenza" - IRCCS -

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

gluten

rice starch

Arm Description

gluten is administered blindly versus placebo for 15 days at 10 g/day

placebo (rice starch) will be administered blindly versus gluten for 15 days at 10 g/day

Outcomes

Primary Outcome Measures

Symptoms evaluation according to 3 scales: score after 2 weeks of gluten ingestion
The evaluation will be made according to the score calculated on the basis of three evaluation scales: "Gastrointestinal Symptom Rating Scale "(GSRS), modified, provides a score ranging MIN=15/MAX=60; Extra-gastrointestinal symptoms evaluation scale, proposed on the basis of the symptoms most frequently observed in GS patients, provides a score ranging MIN=9/MAX=34; VQV scale proposed to evaluate the quality of life, provides a score ranging MIN=16/MAX=64. Total score can be no less than 37 (MIN) and not more than 146 (MAX), with a cut-off of 55.

Secondary Outcome Measures

Bio-Markers to differentiate GS and CD
The identification of possible markers (serological, gut barrier function, immunological and expression of tight junctions constitutive proteins) that may be of help to differentiate, in humans, the condition of gluten sensitivity (GS) from that of Celiac Disease (CD); these markers might be of help in the early diagnosis of GS versus CD especially when the serology is discordant.
Symptoms evaluation according to 3 scales: scores 2 weeks after completion of intervention
The evaluation will be made according to the score calculated on the basis of three evaluation scales: "Gastrointestinal Symptom Rating Scale "(GSRS), modified, provides a score ranging MIN=15/MAX=60; Extra-gastrointestinal symptoms evaluation scale, proposed on the basis of the symptoms most frequently observed in GS patients, provides a score ranging MIN=9/MAX=34; VQV scale proposed to evaluate the quality of life, provides a score ranging MIN=16/MAX=64. Total score can be no less than 37 (MIN) and not more than 146 (MAX), with a cut-off of 55.

Full Information

First Posted
November 17, 2011
Last Updated
April 12, 2016
Sponsor
University of Campania "Luigi Vanvitelli"
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1. Study Identification

Unique Protocol Identification Number
NCT01485341
Brief Title
Gluten Sensitivity in Non-Celiac Patients
Acronym
GS
Official Title
Double Blind Randomized Placebo Controlled Multicenter Trial (Gluten vs Placebo) in Gluten Sensitive Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campania "Luigi Vanvitelli"

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The idea is to evaluate if the so called "Gluten Sensitivity" is a real clinical entity. Gluten sensitive (GS) persons are defined as those patients, being neither celiac or allergic to weat, who develop symptoms following gluten consumption. This will be achieved by evaluating a global symptom score in GS patients receiving gluten compared to those receiving placebo (primary end point). Symptoms to be evaluated: gastrointestinal (Gastrointestinal Symptom Rating Scale, GSRS); not-gastrointestinal (specifically built evaluation scale); VQV scale, built to evaluate quality of life. Gluten or placebo will be administered daily (10 g) for 15 days; for the 15 days before and 15 after all patients will stay on Gluten Free Diet (GFD). Besides clinical evaluation (each week for 6 weeks), intestinal permeability testing and blood sampling will be requested for the identification of possible markers (serological, gut barrier function, immunological and expression of tight junctions constitutive proteins) that may be of help to differentiate the condition of gluten sensitivity (GS) from that of Celiac Disease (CD)(secondary end point). Inclusion and exclusion criteria for patients enrolling are strictly dependant on the given "Gluten sensitivity" definition. We expect to experience a worsening of gastrointestinal and extra-gastrointestinal symptoms, from hours to days, with an increase in the overall symptom score, above the cut off, in at least 45% of GS subjects enrolled and that have received gluten compared to GS who received placebo.
Detailed Description
Gluten is the most important protein component of some grains, notably wheat, rye, and barley, which are the basis for a variety of flour and wheat derived alimentary products consumed throughout the world (bread, pasta, pizza etc). However the "engineering" of gluten-containing grains created the conditions for human diseases related to gluten exposure. These forms of gluten intolerance represent a heterogeneous set of conditions, including wheat allergy, Gluten Sensitivity and Celiac Disease, that, combined, affect about 10% of the general population. The frequency of not-celiac gluten intolerance is however still unknown, even though it is possible that these conditions have been undiagnosed and under-diagnosed by the physicians for long time. The state of immune responsiveness to wheat antigens, represents a complex process, and its establishment and maintenance are not completely elucidated. The most frequent diseases caused by wheat ingestion are T cell-mediated disorders, IgE-mediated allergic reactions and celiac disease (CD). However, besides CD and wheat allergy, there are cases of gluten reactions in which neither allergic nor autoimmune mechanisms are involved. These are generally defined as gluten sensitivity (GS). Some individuals, who experience distress when eating gluten-containing products and show improvement when following a gluten-free diet, may have GS instead of CD. GS patients are unable to tolerate gluten and develop an adverse reaction when eating gluten that usually, and differently from CD, does not lead to small intestinal damage. While the gastrointestinal symptoms in GS may resemble those associated with CD, the overall clinical picture is generally less severe and is not accompanied by the concurrence of tTG autoantibodies or autoimmune disease. Typically the diagnosis is made by exclusion, and an elimination diet and "open challenge" (i.e., the monitored reintroduction of gluten-containing foods) are most often used to evaluate whether health improves with the elimination or reduction of gluten from the diet. This has two major aims: Evaluation of the effective dependence from the gluten of the clinical alterations presented by subjects with gluten sensitivity (GS). The study will be done after a period of gluten-free diet (washout of 15 days), comparing two groups of GS subjects: given gluten or placebo (15 days), followed by a further period (15 days) on gluten free diet . identification of possible markers (serological, gut barrier function, immunological and expression of tight junctions constitutive proteins) that may be of help to differentiate, in humans, the condition of gluten sensitivity (GS) from that of Celiac Disease (CD); these markers might be of help in the early diagnosis of GS versus CD especially in the case of discordant serology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gluten Sensitivity
Keywords
gluten sensitivity

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
108 (Actual)

8. Arms, Groups, and Interventions

Arm Title
gluten
Arm Type
Active Comparator
Arm Description
gluten is administered blindly versus placebo for 15 days at 10 g/day
Arm Title
rice starch
Arm Type
Placebo Comparator
Arm Description
placebo (rice starch) will be administered blindly versus gluten for 15 days at 10 g/day
Intervention Type
Dietary Supplement
Intervention Name(s)
gluten
Intervention Description
gluten is administered once a day at 10g/day for 15 days
Intervention Type
Dietary Supplement
Intervention Name(s)
rice starch
Intervention Description
rice starch is administered once a day at 10 g/day for 15 days
Primary Outcome Measure Information:
Title
Symptoms evaluation according to 3 scales: score after 2 weeks of gluten ingestion
Description
The evaluation will be made according to the score calculated on the basis of three evaluation scales: "Gastrointestinal Symptom Rating Scale "(GSRS), modified, provides a score ranging MIN=15/MAX=60; Extra-gastrointestinal symptoms evaluation scale, proposed on the basis of the symptoms most frequently observed in GS patients, provides a score ranging MIN=9/MAX=34; VQV scale proposed to evaluate the quality of life, provides a score ranging MIN=16/MAX=64. Total score can be no less than 37 (MIN) and not more than 146 (MAX), with a cut-off of 55.
Time Frame
Change from baseline at 2 weeks
Secondary Outcome Measure Information:
Title
Bio-Markers to differentiate GS and CD
Description
The identification of possible markers (serological, gut barrier function, immunological and expression of tight junctions constitutive proteins) that may be of help to differentiate, in humans, the condition of gluten sensitivity (GS) from that of Celiac Disease (CD); these markers might be of help in the early diagnosis of GS versus CD especially when the serology is discordant.
Time Frame
Change from baseline at 2 weeks
Title
Symptoms evaluation according to 3 scales: scores 2 weeks after completion of intervention
Description
The evaluation will be made according to the score calculated on the basis of three evaluation scales: "Gastrointestinal Symptom Rating Scale "(GSRS), modified, provides a score ranging MIN=15/MAX=60; Extra-gastrointestinal symptoms evaluation scale, proposed on the basis of the symptoms most frequently observed in GS patients, provides a score ranging MIN=9/MAX=34; VQV scale proposed to evaluate the quality of life, provides a score ranging MIN=16/MAX=64. Total score can be no less than 37 (MIN) and not more than 146 (MAX), with a cut-off of 55.
Time Frame
Return to baseline values at 4 weeks

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: Adult patients with age between 18-65 with signs/symptoms compatible with gluten-triggered disorders Patients testing negative for celiac disease either by biopsy Marsh 0-1 or those who are HLA-DQ2 and DQ8 negative, as well as tTG and EMA negative Patients that improved on a gluten free diet Exclusion Criteria: Subjects diagnosed with celiac disease (positive TTG and/or EMA, and histology positive with Marsh II or above); Subjects diagnosed with wheat allergy Subjects with Type 1 Diabetes (T1D) Subjects with Inflammatory Bowel Disease (ulcerative colitis or Crohn's disease) Pregnancy Subjects with Helicobacter Pylori infection and other gastrointestinal infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna Sapone, MD, PhD
Organizational Affiliation
University of Campania "Luigi Vanvitelli"
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Celiac Research & Treatment, Yawkey Center for Outpatients Care
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
Università Politecnica delle Marche
City
Ancona
Country
Italy
Facility Name
Gastroenterologia ed Endoscopia digestiva, Ospedale San Giuseppe Moscati
City
Avellino
Country
Italy
Facility Name
Gastroenterology, Second University of Naples
City
Naples
ZIP/Postal Code
80138
Country
Italy
Facility Name
Internal Medicine, Policlinico di Palermo
City
Palermo
Country
Italy
Facility Name
Gastroenterology, University of Salerno
City
Salerno
Country
Italy
Facility Name
Ospedale "Casa Sollievo della Sofferenza" - IRCCS -
City
San Giovanni Rotondo (Foggia)
Country
Italy

12. IPD Sharing Statement

Learn more about this trial

Gluten Sensitivity in Non-Celiac Patients

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