BTO: Validation of Breath Tests in Diagnosing Small Bowel Bacterial Overgrowth

Sponsor
University Hospital, Bonn (Other)
Overall Status
Completed
CT.gov ID
NCT00872092
Collaborator
(none)
22
1
11
2

Study Details

Study Description

Brief Summary

Normally the gastrointestinal tract is only sparsely colonized with bacteria. The normal flora of the duodenal or jejunal aspirate contains no more than 10^5 bacteria per milliliter. Small bowel bacterial overgrowth (SBBO) is defined as a pathologically increased number of bacteria or the presence of colonic flora in the proximal intestine. The reasons for this condition are manifold, ranging from diabetic neuropathy to surgical bypass. SBBO is frequent in elderly people. Therapy is targeted at correcting the underlying small bowel abnormalities that predispose to the condition and at providing appropriate antibiotic therapy. The symptoms and signs of SBBO can be reversed with this approach. However, in many patients the conditions predisposing to SBBO persist life-long, once present. This suggests that noninvasive, sensitive diagnostic tools with high specificity are required. Bacterial culture of upper intestinal content is considered the diagnostic gold standard. However, since endoscopic harvesting of duodenal or jejunal fluid is difficult and invasive, indirect tests such as breath tests have been advocated as diagnostic tools. Hydrogen breath tests are commonly employed since the substrates can be easily obtained and the measurement is simple. Hydrogen is formed when carbohydrates are fermented in the intestine. Breath hydrogen analysis allows a separation of metabolic activity of the intestinal flora from that of the host, since no known hydrogen production occurs in mammalian tissue. The hydrogen breath test most often used in routine clinical practice uses glucose. However, the utility of this test is mostly limited by its low sensitivity, because there are "nonproducers" in up to 25% of the subjects tested. The investigators have developed a stable isotope breath test using 13C-labeled lactose-ureide. Glycosyl-ureides are condensation products of reducing sugars and urea in aqueous acid. Lactose-[13C]ureide has been used to investigate oro-caecal transit time because it resists digestion by small intestinal enzymes and is hydrolyzed by bacterial enzymes in the large intestine. A number of studies have described the use of this substrate in adults and children. The aim of the present study was to investigate the lactose-[13C]ureide breath test in subjects with suspected SBBO and to compare its results with the results of the glucose hydrogen breath test. Microbiological analyses of upper intestinal bacterial cultures were used as gold standard to identify SBBO.

Condition or Disease Intervention/Treatment Phase
  • Other: Stable-isotope labeled lactose ureide breath test

Study Design

Study Type:
Observational
Actual Enrollment :
22 participants
Official Title:
Validation of Breath Tests in Diagnosing Small Bowel Bacterial Overgrowth
Study Start Date :
Oct 1, 1997
Actual Primary Completion Date :
Sep 1, 1998
Actual Study Completion Date :
Sep 1, 1998

Arms and Interventions

Arm Intervention/Treatment
Breath test

Subjects with suspected SBBO

Other: Stable-isotope labeled lactose ureide breath test
2 g 13C-labeled lactose ureide orally
Other Names:
  • Lactosyl ureide
  • Outcome Measures

    Primary Outcome Measures

    1. 13CO2 enrichment in breath CO2 [3 hours]

    Secondary Outcome Measures

    1. Hydrogen output in breath [3 hours]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Suspected small bowel bacterial overgrowth
    Exclusion Criteria:
    • Age < 18 years

    • Antibiotic therapy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Bonn Bonn Germany 53105

    Sponsors and Collaborators

    • University Hospital, Bonn

    Investigators

    • Principal Investigator: Heiner K. Berthold, MD, PhD, University of Bonn

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00872092
    Other Study ID Numbers:
    • BTO-0001
    First Posted:
    Mar 31, 2009
    Last Update Posted:
    Mar 31, 2009
    Last Verified:
    Mar 1, 2009
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 31, 2009