To Evaluate Improvement Effect of Subjective Symptoms of Mucotra SR Tablet in Patients With Gastritis
NCT06668506 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2814
Last updated 2024-11-04
Summary
This study aims to evaluate the improvement effect on subjective symptoms of gastritis and adverse events through patient self-assessment results (PRO) by conducting follow-up observations for patients with gastritis at 2 to 4 weeks after administration of Mucotra® SR tablets.
Conditions
- Gastritis
Sponsors & Collaborators
-
Daewoong Pharmaceutical Co. LTD.
lead INDUSTRY
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-03-17
- Primary Completion
- 2022-11-03
- Completion
- 2024-03-13
Countries
- South Korea
Study Locations
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