A Study to Evaluate the Improvement Effect on Subjective Symptom of

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

This observation study is a large-scale, prospective, and multi-organ observation study to observe the improvement effect of the self-evaluation results (PRO) of erosive gastroesophageal reflux disease at least 4 to 8 weeks after administration of Fexuclue Tab. Subjects who met the inclusion/exclusion criteria will administer Fexuclue Tablet once a day for four weeks after registration, regardless of their meals. If esophagitis is not treated or symptoms continue after 4 weeks of administration, the subject will continue to administer Fexuclue Tablet for 4 more weeks (maximum administration period: 8 weeks). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05660122
Study type	Observational
Source	Daewoong Pharmaceutical Co. LTD.
Contact	HyeongSeon Noh
Phone	8210-4266-0549
Email	hsno116@daewoong.co.kr
Status	Recruiting
Phase
Start date	November 11, 2022
Completion date	October 31, 2023

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A Study to Evaluate the Improvement Effect on Subjective Symptom of FEXUCLUE Tab

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms