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Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study

Primary Purpose

Fructose Intolerance

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Placebo
Alanine
Alanine
Sponsored by
Augusta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fructose Intolerance

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age between 18-70 years
  2. Diagnosis of fructose malabsorption (positive breath test after ingestion of 25 grams of fructose defined as either (a) ≥ 20 ppm rise of breath H2/CH4/both over baseline values or a successive rise of ≥ 5 ppm over baseline and in 3 consecutive breath samples)

Exclusion Criteria:

  1. Cognitive impairment or any other inability to provide informed consent
  2. Prisoners
  3. GI surgery except appendectomy, cholecystectomy, caesarean section, hysterectomy
  4. Antibiotics in the previous 3 months
  5. Bacterial overgrowth or lactose intolerance
  6. Major co-morbid illnesses, including chronic pancreatitis, celiac disease, inflammatory bowel disease, diabetes, scleroderma, pseudo-obstruction syndromes etc.
  7. Known food allergies
  8. Medication use: opioids, Tegaserod, laxatives, enemas
  9. Diabetes

Sites / Locations

  • University of Iowa Hospitals and ClinicsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

Placebo

Alanine - 12.5

Alanine - 25

Arm Description

Subjects will receive placebo (mix of sugar and salt).

Subjects will receive 12.5 grams of alanine

Subjects will receive 25 grams of alanine.

Outcomes

Primary Outcome Measures

Decrease breath Hydrogen and/or Methane production

Secondary Outcome Measures

Occurrence or severity of GI symptoms during the test

Full Information

First Posted
September 22, 2009
Last Updated
July 19, 2022
Sponsor
Augusta University
Collaborators
University of Iowa, Teikyo University
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1. Study Identification

Unique Protocol Identification Number
NCT01185210
Brief Title
Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study
Official Title
Investigation of Alanine in Fructose Intolerance: A Randomized, Double Blind, Dose Ranging, Placebo Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 2007 (undefined)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Augusta University
Collaborators
University of Iowa, Teikyo University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Over the past few decades, fructose is increasingly being used as a sweetener/ additive in a variety of foods. Incomplete absorption of fructose has been implicated as a cause of gastrointestinal symptoms. In tertiary care centers, the prevalence of fructose malabsorption in subjects with unexplained GI symptoms is thought to be between 11-50%, when assessed with breath tests following administration of 25 grams of fructose in a 10% solution. Restriction of dietary fructose has been shown to improve symptoms in these patients to an extent. Currently, there are no therapeutic agents that improve intestinal fructose absorption and thereby decrease symptoms. Studies in the pediatric population have shown that fructose absorption in the small intestine is increased in the presence of glucose or amino acids, especially alanine. Objective: The investigators' objective is to assess whether co-administration of an oral solution of L-alanine facilitates fructose absorption and decreases gastrointestinal (GI) symptoms associated with fructose malabsorption in subjects undergoing standard fructose breath test when compared to placebo. Methods and analysis: The investigators propose a randomized, double-blind study in 40 subjects with known fructose intolerance. After an overnight fast, each subject will receive an oral solution of 12.5 grams of alanine in 125cc of water or placebo. Next, the subject will receive an oral solution of 25 grams of fructose in a 10% solution. Serum, urine and breath samples will be collected at baseline and at 30-minute intervals for 4 hours. GI symptoms will also be assessed and recorded at 30 minute intervals using a standard questionnaire. Repeated measures ANOVA will be used to compare the data obtained during the study protocol with the baseline (pre-study) data. Expected outcomes: Co-administration of alanine with fructose may improve fructose absorption and decrease symptoms in subjects with fructose intolerance. Hypothesis: Ingestion of alanine along with fructose, will facilitate intestinal absorption of fructose in subjects with fructose malabsorption. Aim: To investigate the effects of co-administration of equi-molar doses of alanine on a) the absorption of fructose and b) the occurrence of GI symptoms in subjects with fructose malabsorption.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fructose Intolerance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Subjects will receive placebo (mix of sugar and salt).
Arm Title
Alanine - 12.5
Arm Type
Experimental
Arm Description
Subjects will receive 12.5 grams of alanine
Arm Title
Alanine - 25
Arm Type
Experimental
Arm Description
Subjects will receive 25 grams of alanine.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Subjects will receive placebo (mix of sugar and salt) 20 minutes before consuming fructose.
Intervention Type
Dietary Supplement
Intervention Name(s)
Alanine
Intervention Description
Subjects will receive 12.5 grams of alanine 20 minutes before consuming fructose.
Intervention Type
Dietary Supplement
Intervention Name(s)
Alanine
Intervention Description
Subjects will receive 25 grams of alanine 20 minutes before consuming fructose.
Primary Outcome Measure Information:
Title
Decrease breath Hydrogen and/or Methane production
Time Frame
less than 6 months
Secondary Outcome Measure Information:
Title
Occurrence or severity of GI symptoms during the test
Time Frame
less than 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-70 years Diagnosis of fructose malabsorption (positive breath test after ingestion of 25 grams of fructose defined as either (a) ≥ 20 ppm rise of breath H2/CH4/both over baseline values or a successive rise of ≥ 5 ppm over baseline and in 3 consecutive breath samples) Exclusion Criteria: Cognitive impairment or any other inability to provide informed consent Prisoners GI surgery except appendectomy, cholecystectomy, caesarean section, hysterectomy Antibiotics in the previous 3 months Bacterial overgrowth or lactose intolerance Major co-morbid illnesses, including chronic pancreatitis, celiac disease, inflammatory bowel disease, diabetes, scleroderma, pseudo-obstruction syndromes etc. Known food allergies Medication use: opioids, Tegaserod, laxatives, enemas Diabetes
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Satish SC Rao, MD
Phone
319-353-6602
Email
satish-rao@uiowa.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Satish Rao, Md, PhD
Organizational Affiliation
University of Iowa
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Iowa Hospitals and Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Satish SC Rao, MD
Phone
319-353-6602
Email
satish-rao@uiowa.edu

12. IPD Sharing Statement

Learn more about this trial

Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study

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