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Status unknownNCT01185210Updated Jul 21, 2022

Investigation of Alanine in Fructose Intolerance: A Dose Ranging Study

An interventional study of Placebo and Alanine in Fructose Intolerance, sponsored by Augusta University. Status unknown at 1 site in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2022-07-21.

Sponsored by Augusta University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Fructose Intolerance
03

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
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

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
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
100 participants (estimated)

Study arms

  • Placebo comparator
    Placebo

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

    Dietary Supplement: Placebo

  • Experimental
    Alanine - 12.5

    Subjects will receive 12.5 grams of alanine

    Dietary Supplement: Alanine

  • Experimental
    Alanine - 25

    Subjects will receive 25 grams of alanine.

    Dietary Supplement: Alanine

Interventions

  • Dietary supplementPlacebo

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

  • Dietary supplementAlanine

    Subjects will receive 12.5 grams of alanine 20 minutes before consuming fructose.

  • Dietary supplementAlanine

    Subjects will receive 25 grams of alanine 20 minutes before consuming fructose.

05

What researchers measure

Primary outcomes

  1. Decrease breath Hydrogen and/or Methane production

    Time frame: less than 6 months

Secondary outcomes

  1. Occurrence or severity of GI symptoms during the test

    Time frame: less than 6 months

06

Study locations

1 of 1 sites recruiting
  • University of Iowa Hospitals and Clinics
    Iowa City, Iowa 52242, United States
    Recruiting
07

Registry details

Key details

Study ID
NCT01185210
Lead sponsor
Augusta University
Collaborators
University of Iowa, Teikyo University
Responsible party
Satish Rao (Professor, Augusta University) — Principal investigator
First posted
Aug 19, 2010
Start date
Sep 2007
Primary completion
Dec 31, 2023 (estimated)
Completion
Apr 30, 2024 (estimated)
Last update
Jul 21, 2022

Study contacts

Satish SC Rao, MD
Contact
satish-rao@uiowa.edu
319-353-6602
Satish Rao, Md, PhD
principal investigator · University of Iowa

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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