Skip to content

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

Observational Study to Evaluate Effectiveness, Safety and Satisfaction Level of Zastaprazan (JAQBO®) Under Daily Treatment for Patients With Erosive Gastroesophageal Reflux Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06952855
Enrollment
5536
Registered
2025-05-01
Start date
2024-11-01
Completion date
2025-04-23
Last updated
2025-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acid Regurgitation, Erosive Reflux Disease, Heartburn

Keywords

GERD, ERD

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.

Interventions

None listed

Sponsors

Jeil Pharmaceutical Co., Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in GERD (heartburn, acid regurgitation) score in RDQ4 weeksScale(none / 1day / 2day/ 3-4 day / 5-6 day/ every day)

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026