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Clinical Trial Summary

This observational study is a large-scale, prospective, and multi-institutional observational study. Patients from 19 to 75 years of age, will take a self-assessment (PRO) during the study period before and after administration of Pexuclue tablet.


Clinical Trial Description

Data will be collected based on patient's medical records from daily visit. Enrolled subjects will take a Patient Reported Outcome (PRO) survey including Quality of life evaluation (GERD-HRQL) and self-awareness symptom (RDQ). The survey will be done twice (before and after the administration of Fexuclue tablet) electronically through an application (e-PRO). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05614752
Study type Observational
Source Daewoong Pharmaceutical Co. LTD.
Contact
Status Active, not recruiting
Phase
Start date July 6, 2022
Completion date December 31, 2024

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