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Observationa Study is a Prospective and Multi-institutional Observational Study.

Completed
Conditions
Erosive Reflux Disease
Heartburn
Acid Regurgitation
Registration Number
NCT06952855
Lead Sponsor
Jeil Pharmaceutical Co., Ltd.
Brief Summary

This observational study is a prospective, multi-institutional non intervention study to examine the prescription patterns, corresponding treatment effects and safety in routine clinical practice for patients prescribed for the treatment of gastroesophageal reflux disease.

Detailed Description

The present observational study is designed to check effect and safety for patients who have been prescribed JAQBO for the treatment of erosive gastroesophageal reflux disease.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5536
Inclusion Criteria
  1. An adult over 19 years of age
  2. A person who voluntarily provides written informed consent
Exclusion Criteria
  1. A pregnant woman or a nursing woman
  2. A person who is deemed unsuitable for the subject of the study

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in GERD (heartburn, acid regurgitation) score in RDQ4 weeks

Scale(none / 1day / 2day/ 3-4 day / 5-6 day/ every day)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Goodbreath Medical Center

🇰🇷

Seoul, Gyeonggi-do, Korea, Republic of

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