This study is to evaluate the efficacy and safety of DA-5219 in patients with acute or chronic gastritis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
467
Asan Medical Center
Seoul, South Korea
Improvement rate of gastric mucosal erosion
Time frame: Change from baseline at 2 weeks
Cure rate for gastric mucosal erosion
Time frame: Change from baseline at 2 weeks
Cure rate for gastric mucosal edema
Time frame: Change from baseline at 2 weeks
Improvement rate for gastric mucosal erythema
Time frame: Change from baseline at 2 weeks
Improvement rate for gastric mucosal bleeding
Time frame: Change from baseline at 2 weeks
Improvement rate for gastric subjective symptoms
Time frame: Change from baseline at 2 weeks
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3 tablets/day