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MSG and Gastrointestinal Motility

Primary Purpose

Gastroesophageal Reflux

Status
Completed
Phase
Not Applicable
Locations
Japan
Study Type
Interventional
Intervention
Monosodium glutamate
Sodium chloride
Sponsored by
Gunma University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Gastroesophageal Reflux focused on measuring Gastrointestinal motility, Gastroesophageal reflux, Gastric emptying, Sodium glutamate, Lower esophageal sphincter

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy subjects
  • Must not have digestive symptoms
  • Must not eat within six hours of study participation

Exclusion Criteria:

  • Regular medications for the gastrointestinal tract
  • Previous Helicobacter pylori infection
  • Previous abdominal surgery

Sites / Locations

  • Gunma university hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

MSG first

NaCl first

Arm Description

Outcomes

Primary Outcome Measures

Gastric emptying
half emptying time

Secondary Outcome Measures

Full Information

First Posted
November 6, 2009
Last Updated
March 25, 2015
Sponsor
Gunma University
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1. Study Identification

Unique Protocol Identification Number
NCT01009658
Brief Title
MSG and Gastrointestinal Motility
Official Title
Effect of Monosodium Glutamate on Upper Gastrointestinal Tract Motility
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

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

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to clarify the physiological function of sodium glutamate by measuring its effect on upper GI motility ( gastric emptying).
Detailed Description
Amino acids such as monosodium glutamate are known to stimulate both endocrine and exocrine secretion. In addition, there is a report that oral intake of glutamate evokes the activation of vagal afferent nerves in the rat. Thus, such amino acids are thought to be influential in the process of digestion and absorption. . To investigate the effect of monosodium glutamate on gastrointestinal motility, we planned a single-blind randomized study. The participants will take either monosodium glutamate or sodium chloride before the first examination of upper GI motility and the other agent before the second examination. The order of intake will be randomized by the envelope method.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux
Keywords
Gastrointestinal motility, Gastroesophageal reflux, Gastric emptying, Sodium glutamate, Lower esophageal sphincter

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MSG first
Arm Type
Active Comparator
Arm Title
NaCl first
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Monosodium glutamate
Intervention Description
Oral intake of 2.0 g of monosodium glutamate on the examination day and 0.6 g of sodium chloride on the other examination day.
Intervention Type
Dietary Supplement
Intervention Name(s)
Sodium chloride
Intervention Description
Oral intake of 0.6 g of sodium chloride on the examination day and 2.0 g of monosodium glutamate on the other examination day.
Primary Outcome Measure Information:
Title
Gastric emptying
Description
half emptying time
Time Frame
0-5 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy subjects Must not have digestive symptoms Must not eat within six hours of study participation Exclusion Criteria: Regular medications for the gastrointestinal tract Previous Helicobacter pylori infection Previous abdominal surgery
Facility Information:
Facility Name
Gunma university hospital
City
Maebashi
State/Province
Gunma
ZIP/Postal Code
3718511
Country
Japan

12. IPD Sharing Statement

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