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Study on medical treatment for patients with reflux esophagitis refractory to proton pump inhibitor

Not Applicable
Conditions
Reflux esophagitis
Registration Number
JPRN-UMIN000003911
Lead Sponsor
Department of Gastroenterology, Kobe University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Patients with the past history of digestive tract excisio and vagotomy (2) Patients who have alert symptoms such as nausea, gastrointestinal bleeding and rapid weight loss (3) Patients who have past history of or suffer from the following diseases: Zollinger-Ellison symdrome, inflammatory bowel disease, esophageal stenosis, achalasia, malabsorption, cerebrovascular disease such as cerebral hemorrhage or cerebral infarction (4) Patients having severe liver, kidney or heart disease (5) Patients who have malignancy or are suspected of having malignancy (6) Patients who are pregnant, in breast-feeding or may have cecome pregnant (7) Patients who need continuous medication of atazanavir sulfate, diazepam, phenytoin, warfarin, tacrolimus, digoxin, methyldigoxin, itraconazole, Gefinitinib or voriconazole that might interact with the test drug (8) Patients who are receiving proton pump inhibitors except rabeprazole (9) Patients whom the doctor in charge judged to be unsuitable as an object of this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in scores of Frequency scale for symptoms of gastroesophageal reflux diseases (FSSG)
Secondary Outcome Measures
NameTimeMethod
1)Changes in scores of gastrointestinal symptom rating scale (GSRS) 2)Subgroup analysis for CYP2C19 genotype
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