Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study

Sponsor
Augusta University (Other)
Overall Status
Recruiting
CT.gov ID
NCT01185210
Collaborator
University of Iowa (Other), Teikyo University (Other)
100
1
3
200
0.5

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Placebo
  • Dietary Supplement: Alanine
  • Dietary Supplement: Alanine
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Investigation of Alanine in Fructose Intolerance: A Randomized, Double Blind, Dose Ranging, Placebo Controlled Study
Study Start Date :
Sep 1, 2007
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

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

Dietary Supplement: Placebo
Subjects will receive placebo (mix of sugar and salt) 20 minutes before consuming fructose.

Experimental: Alanine - 12.5

Subjects will receive 12.5 grams of alanine

Dietary Supplement: Alanine
Subjects will receive 12.5 grams of alanine 20 minutes before consuming fructose.

Experimental: Alanine - 25

Subjects will receive 25 grams of alanine.

Dietary Supplement: Alanine
Subjects will receive 25 grams of alanine 20 minutes before consuming fructose.

Outcome Measures

Primary Outcome Measures

  1. Decrease breath Hydrogen and/or Methane production [less than 6 months]

Secondary Outcome Measures

  1. Occurrence or severity of GI symptoms during the test [less than 6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Iowa Hospitals and Clinics Iowa City Iowa United States 52242

Sponsors and Collaborators

  • Augusta University
  • University of Iowa
  • Teikyo University

Investigators

  • Principal Investigator: Satish Rao, Md, PhD, University of Iowa

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Satish Rao, Professor, Augusta University
ClinicalTrials.gov Identifier:
NCT01185210
Other Study ID Numbers:
  • Fructose: Double Blind
First Posted:
Aug 19, 2010
Last Update Posted:
Jul 21, 2022
Last Verified:
Jul 1, 2022
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 21, 2022