Status:
WITHDRAWN
Comparative Study of Epigastric Pain Syndrome and Postprandial Distress Syndrome
Lead Sponsor:
National Taiwan University Hospital
Conditions:
Functional Dyspepsia
Epigastric Pain Syndrome
Eligibility:
All Genders
20+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare postprandial distress syndrome and epigastric pain syndrome in demographics psychological features, infection of Helicobacter pylori, gastric emptying and thera...
Detailed Description
Functional dyspepsia is a common clinical disorder with significant impact on quality of life and with enormous social cost. Previous studies have revealed that functional dyspepsia is not a homogenou...
Eligibility Criteria
Inclusion
- aged greater than 20 years
- fulfill Rome III diagnostic criteria
Exclusion
- children and teenagers aged less than 20 years
- Organic lesions such as ulcers, tumors, bleeding, vasculopathy or esophagitis as demonstrated on upper endoscopy
- concurrent illness with malignancy, diabetes mellitus, liver cirrhosis, renal failure or porphyria
- diagnosis of organic disease for dyspeptic symptoms by treating physicians
- history of abdominal surgery
- concurrent user of aspirin and NSAID
- history of allergy or severe side effects to lansoparzole
- pregnant or lactating women
Key Trial Info
Start Date :
April 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2009
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT00673972
Start Date
April 1 2008
End Date
December 1 2009
Last Update
March 10 2010
Active Locations (1)
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1
National Taiwan University Hospital
Taipei, Taiwan, 100