Does Small Intestinal Bacterial Overgrowth Contribute to Functional Dyspepsia
Completed · Not applicable · Has a placebo group
Conditions studied: Functional Dyspepsia, Small Intestinal Bacterial Overgrowth, Chronic Abdominal Discomfort
In brief
The prevalence of functional dyspepsia (FD) is estimated to be 15% of the adult population. FD is commonly described as a condition of chronic abdominal discomfort localized to the upper abdomen. Postprandial bloating, pain, nausea, vomiting, belching, and early satiety are common symptoms of the FD patient. FD is defined by \>12 weeks of symptoms, which need not be consecutive, within the preceding year consisting of a) persistent or recurrent dyspepsia and b) an absence of organic disease after a gastrointestinal endoscopy or x-ray series. FD is therefore considered a disorder of function because no mucosal pathology is seen in these patients, as in patients with other functional disorders such as irritable bowel syndrome (IBS) and fibromyalgia (FM). There is a remarkable degree of overlap among these three disorders. These 3 disorders share the finding of hypersensitivity and the symptom of postprandial bloating to suggest the possibility of a common origin.
Key facts
- Study ID
- NCT00956397
- Run by
- Henry C. Lin, MD
- People needed
- 55
- Starts
- 2007-08-01
- Last updated by the study team
- 2012-10-24
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must have FD based on the most recent Umbrella criteria of one or more of: a. bothersome postprandial fullness, b. early satiation, c. epigastric pain, d. epigastric burning
- No evidence of organic disease (including H. pylori detected at time of endoscopy) that is likely to explain the symptoms
- Criteria must be fulfilled for the last 3 months with symptom onset at least 6 months before the diagnosis
- The physical exam, routine blood tests including CBC, chemistry panel and liver tests, upper gastrointestinal endoscopy and 24h pH study must be normal
You may not qualify if…
- History of IBS,rheumatoid arthritis,H. Pylori infection,lupus,peptic ulcer, cirrhosis,diabetes, HIV or TB
- Inflammatory bowel disease
- Bowel Resection (including gastric, small bowel or colon; gallbladder surgery or appendectomy are NOT exclusion criteria)
- Anti/pro-biotics last 3 months
- Previous LBT (Lactulose Breath Test)
- Narcotic Dependence
- Pregnancy
- Control subjects will be excluded if they have symptoms of heartburn, retrosternal chest pain, chronic cough, nausea or regurgitation suggestive of gastroesophageal reflux disease
Where it is running
- General Clinical Research Center — Albuquerque, New Mexico, United States
Full record on ClinicalTrials.gov
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