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Study of symptom improvement effect of gastric acid suppressive drugs in reflux esophagitis patients -a randomized comparative study of vonoprazan vs esomeprazole

Not Applicable
Conditions
Reflux esophagitis
Registration Number
JPRN-UMIN000022166
Lead Sponsor
Department of Gastroenterology, Sapporo-kosei General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients with warning signs such as vomiting, gastrointestinal bleeding (including findings of hematemesis, melena, and anemia), and sudden weight loss 2.Patients confirmed or suspected malignant lesion 3.Patients with a history of gastrointestinal resection or vagotomy 4.Patients in Irritable Bowel Syndrome 5.Patients whose participation in this study would be contraindicated due to complications such as serious hepatic disease, renal disease, or cardiac disease. 6.Women who are pregnant or who may possibly be pregnant, and lactating mothers 7.Other patients whom the investigator considers unsuitable for admission to the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Gerd Q total score of heartburn and acid regurgitation
Secondary Outcome Measures
NameTimeMethod
1.Gerd Q each score of heartburn and acid regurgitation 2.Gerd Q each score of epigastralgia, nausea and vomiting 3.Evaluation of treatment response with Gerd Q
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