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To Evaluate Improvement Effect of Subjective Symptoms of Mucotra SR Tablet in Patients With Gastritis

NCT06668506 COMPLETED

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.

Details

Lead sponsorDaewoong Pharmaceutical Co. LTD.
StatusCOMPLETED
Enrolment2814
Start dateThu Mar 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed Mar 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Countries

South Korea