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Bacterial Overgrowth Associated With Chronic Multisymptom Illness Complex

Bacterial Overgrowth Associated With Chronic Multisymptom Illness Complex

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00956150
Enrollment
210
Registered
2009-08-11
Start date
2009-04-30
Completion date
Unknown
Last updated
2013-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gulf War Syndrome

Keywords

Chronic Multisymptom Complex, Small Intestinal Bacterial Overgrowth, Gulf War Syndrome, Chronic Multisymptom Illness Complex

Brief summary

The adverse impact of Gulf War Syndrome (GWS) on the health of veterans and on the resources of the VA Healthcare System underscores the need to resolve its underlying cause. In response, the investigators propose to investigate the central hypothesis that gut bacteria may be responsible for symptoms associated with GWS. The investigators will enroll a total of 120 patients with GWS and 90 healthy controls.

Detailed description

The investigator will assess the prevalence and role of abnormal gut microbial fermentation among Veterans with GWS and investigate the efficacy of diagnostic and treatment strategies directed at indigenous gut microbes in the management of GWS.

Interventions

Test will begin with a baseline breath sample followed by ingestion of 10g of lactulose (Xactdose, South Beloit, IL) in 100ml of water. Breath samples will be collected every 15 min for 180 min. Gas samples will be analyzed for hydrogen and methane using a gas chromatograph (Model SC, Quintron Instruments, Milwaukee, WI).

DRUGPlacebo

Placebo TID PO x 10 days

DRUGRifaximin

Rifaximin 600 mg three times a day by mouth (TID PO) x 10 days

Sponsors

Henry C. Lin, MD
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Gulf War Veterans meeting the 1994 Centers for Disease Control and Prevention (CDC) criteria for the diagnosis of Chronic Fatigue Syndrome(CFS), i.e \> six months of one or more symptoms from at least two of the following three clusters: general fatigue, mood and cognitive abnormalities, and musculoskeletal pain * Must be under the care of a primary physician and have had a previous diagnosis of Gulf War-related illness or GWS and have medical records documenting investigations to rule out other causes of fatigue * Minimum of the following laboratory screening tests: complete blood count with leukocyte differential, erythrocyte sedimentation rate, serum electrolytes, calcium, glucose, blood urea nitrogen, creatinine,urinalysis, and thyroid function tests * Subjects must also have a GI consult first as part of routine care to confirm eligibility and availability * Patients with Irritable Bowel Syndrome (IBS), fibromyalgia (FM), anxiety or depression will not be excluded, but will be identified for subgroup analysis * Healthy controls will be screened with complete blood count (CBC) and comprehensive metabolic panel to confirm eligibility

Exclusion criteria

* History of peptic ulcer, inflammatory bowel disease, diabetes, cirrhosis, rheumatoid arthritis, lupus, narcotic dependence,celiac disease, tropical sprue, bowel resection(including gastric, small bowel or colon; but gallbladder surgery or appendectomy are NOT

Design outcomes

Primary

MeasureTime frame
To compare the pattern of bacterial gas excretion in breath among Veterans with Gulf War Syndrome vs. Controls using Lactulose Breath Testevery 15 minutes for 180 minutes
To determine the response to antibiotic treatment in Gulf War Syndrome patients.Two weeks

Countries

United States

Contacts

Primary ContactNatalie R Mills, BS
Natalie.Mills@va.gov505-265-1711
Backup ContactHenry C Lin, MD
helin@salud.unm.edu505-265-1711

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026