Gastroesophageal Reflux Disease Clinical Trial
Official title:
Diagnostic Efficacy of Narrow Band Imaging (NBI) in Patients With Gastroesophageal Reflux Disease (GERD)
Verified date | April 2009 |
Source | National Taiwan University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Department of Health |
Study type | Observational |
Gastroesophageal reflux disease (GERD) is a common disorder in Asia that includes erosive and non-erosive counterparts. The evaluation of intra-esophageal damage is of paramount importance because patients with erosive and those with non-erosive GERD have distinct manifestations and prognoses. Although proton-pump inhibitor (PPI) is the treatment of choice for erosive patients with excellent therapeutic response, the majority of reflux patients can be classified with non-erosive reflux disease (NERD).Narrow-band imaging (NBI) is a novel, noninvasive optical technique that adjusts reflected light to improve the contrast of capillary patterns compared with conventional illumination. Based on the standard procedure of sequential conventional white-light, NBI, and magnified NBI, the investigators have validated the reliability of the diagnostic testing. The investigators will also enroll NERD patients to test their therapeutic response to rabeprazole. The investigators can find out the best strategy to identify the PPI responder.
Status | Completed |
Enrollment | 80 |
Est. completion date | April 2009 |
Est. primary completion date | April 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years to 70 Years |
Eligibility |
Inclusion Criteria: 1. Symptomatic reflux subjects who receive esophagogastroscopy, aged from 20 to 70 years old. 2. Patients with typical reflux symptoms (heartburn and/or acid regurgitation) at least 3 times per week in recent 4 months. Exclusion Criteria: 1. Symptomatic reflux patients with apparent erosive esophagitis in conventional endoscopy. 2. Symptomatic reflux patients with a history of using PPI in recent 4 months. 3. Subjects with known allergy to PPI. 4. Peptic ulcer disease 5. Cancers of the esophagus, stomach, and duodenum 6. Esophageal varices. 7. Active upper gastrointestinal bleeding within 7 days prior to enrollment 8. Status after total or subtotal gastrectomy 9. Use of anticoagulants or antiplatelets within one week prior to enrollment 10. Subjects with bleeding tendency |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Taiwan | National Taiwan University Hospital | Taipei |
Lead Sponsor | Collaborator |
---|---|
National Taiwan University Hospital |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Therapeutic response to proton-pump inhibitor (PPI) | 14 days | No |
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