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Clinical Trial Examining Effects of Monosodium Glutamate (MSG) on Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM)

Primary Purpose

Irritable Bowel Syndrome, Fibromyalgia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Glutamate additive-free diet
Placebo diet
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Irritable Bowel Syndrome focused on measuring Irritable Bowel Syndrome, Fibromyalgia, Glutamate, Diet, Food additives

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women aged 18-75 who fulfill criteria for Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM)
  • They must live in the greater Portland, OR, metro area, have transportation to/from study site, have access to email
  • Willing to discontinue medications with bowel altering side effects

Exclusion Criteria:

  • Asthma
  • Inflammatory bowel disease
  • Colon cancer or active endometriosis
  • Any major abdominal surgery (excluding caesarean section, tubal ligation, hernia repair, gall bladder removal or appendectomy)
  • Female and pregnant
  • Currently taking pregabalin, gabapentin, or anti-psychotic medications and are unwilling/ unable to discontinue use
  • Suffered from alcohol/substance abuse or psychosis in the last two years.

Sites / Locations

  • Oregon Health & Science University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1 - Glutamate challenge

2- Placebo

Arm Description

Glutamate challenge: After the one month glutamate free diet, subjects will receive 5 grams of glutamate for three days on one week and placebo for three days on the next week. Arm 1 is the 5 grams of glutamate which will be given in a mixed juice.

Glutamate challenge: After the one month glutamate free diet, subjects will receive 5 grams of glutamate for three days on one week and placebo for three days on the next week. Arm 2 is the placebo arm, which will be juice with nothing added.

Outcomes

Primary Outcome Measures

To evaluate the number of patients who have a positive response to a one month glutamate free diet, as measured by the Perception of Global Impression of Change (PGIC) scores
To assess whether symptoms return with MSG challenge statistically more frequently than with placebo as measured by symptom scores.

Secondary Outcome Measures

Improvement on Irritable Bowel Syndrome-Quality of Life (IBS-QOL) questionnaire
Improvement in day-to-day functioning based on the Revised Fibromyalgia Impact Questionnaire
A reduction in pain based on two visual analog scales, one for gut pain, and another for musculo-skeletal pain

Full Information

First Posted
January 23, 2009
Last Updated
December 21, 2013
Sponsor
Oregon Health and Science University
Collaborators
University of Arizona
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1. Study Identification

Unique Protocol Identification Number
NCT00829218
Brief Title
Clinical Trial Examining Effects of Monosodium Glutamate (MSG) on Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM)
Official Title
A Clinical Trial Examining the Effects of the Food Additive Glutamate on Irritable Bowel Syndrome and Fibromyalgia
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
January 2009 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
May 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
University of Arizona

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objective: Randomized, double blind, placebo-controlled, crossover, clinical trial to examine the effects of the food additive glutamate (in the form of MSG) on IBS and fibromyalgia. Setting and Subjects: The Fibromyalgia Research Database at OHSU will be utilized to identify and recruit fibromyalgia patients who also have IBS to OHSU study centers. Intervention: Approximately 60 male and female subjects aged 18-75 will be placed on a 1-month glutamate-free elimination diet. Those that respond positively to the diet (we are estimating 30-40 subjects), will then be randomized to receive either a citrus drink containing 5 grams of MSG; or placebo (the citrus drink alone)on three consecutive days one week apart. The investigators are hypothesizing that those who react positively to the elimination diet will have symptom occurrence statistically more frequently when given the glutamate challenge, than when given placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome, Fibromyalgia
Keywords
Irritable Bowel Syndrome, Fibromyalgia, Glutamate, Diet, Food additives

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 - Glutamate challenge
Arm Type
Active Comparator
Arm Description
Glutamate challenge: After the one month glutamate free diet, subjects will receive 5 grams of glutamate for three days on one week and placebo for three days on the next week. Arm 1 is the 5 grams of glutamate which will be given in a mixed juice.
Arm Title
2- Placebo
Arm Type
Placebo Comparator
Arm Description
Glutamate challenge: After the one month glutamate free diet, subjects will receive 5 grams of glutamate for three days on one week and placebo for three days on the next week. Arm 2 is the placebo arm, which will be juice with nothing added.
Intervention Type
Other
Intervention Name(s)
Glutamate additive-free diet
Other Intervention Name(s)
Glutamate will be used as a challenge in the form of MSG.
Intervention Description
All subjects will follow a diet for one month where all foods containing the additive glutamate have been removed. At the end of the one month diet, subjects who have responded positively to the diet will go onto the challenge arms of the study, where they will be randomized to receive placebo (mixed juice alone) for three days on one week, and 5 grams of glutamate in the mixed juice for three days on the other week.
Intervention Type
Other
Intervention Name(s)
Placebo diet
Intervention Description
Juice with nothing added.
Primary Outcome Measure Information:
Title
To evaluate the number of patients who have a positive response to a one month glutamate free diet, as measured by the Perception of Global Impression of Change (PGIC) scores
Time Frame
4 weeks
Title
To assess whether symptoms return with MSG challenge statistically more frequently than with placebo as measured by symptom scores.
Time Frame
6 weeks, 7 weeks
Secondary Outcome Measure Information:
Title
Improvement on Irritable Bowel Syndrome-Quality of Life (IBS-QOL) questionnaire
Time Frame
4 weeks, 7 weeks
Title
Improvement in day-to-day functioning based on the Revised Fibromyalgia Impact Questionnaire
Time Frame
4 weeks, 7 weeks
Title
A reduction in pain based on two visual analog scales, one for gut pain, and another for musculo-skeletal pain
Time Frame
4 weeks, 7 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women aged 18-75 who fulfill criteria for Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM) They must live in the greater Portland, OR, metro area, have transportation to/from study site, have access to email Willing to discontinue medications with bowel altering side effects Exclusion Criteria: Asthma Inflammatory bowel disease Colon cancer or active endometriosis Any major abdominal surgery (excluding caesarean section, tubal ligation, hernia repair, gall bladder removal or appendectomy) Female and pregnant Currently taking pregabalin, gabapentin, or anti-psychotic medications and are unwilling/ unable to discontinue use Suffered from alcohol/substance abuse or psychosis in the last two years.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Douglas Taren, PhD
Organizational Affiliation
University of Arizona
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Kathleen F Holton, MPH, PhDc
Organizational Affiliation
University of Arizona and Oregon Health & Science Univ.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kimberly D Jones, PhD
Organizational Affiliation
Oregon Health and Science University
Official's Role
Study Director
Facility Information:
Facility Name
Oregon Health & Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97238
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22766026
Citation
Holton KF, Taren DL, Thomson CA, Bennett RM, Jones KD. The effect of dietary glutamate on fibromyalgia and irritable bowel symptoms. Clin Exp Rheumatol. 2012 Nov-Dec;30(6 Suppl 74):10-7. Epub 2012 Dec 14.
Results Reference
result

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Clinical Trial Examining Effects of Monosodium Glutamate (MSG) on Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM)

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