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Efficacy and Safety of FEXUCLUE Tab. In Patients With Acute or Chronic Gastritis

Recruitingn/aAges 19 Years - 75 YearsAllDaewoong Pharmaceutical Co. LTD.
NCT06948487 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study aims to evaluate the efficacy of Fexuclue tablets in improving gastrointestinal symptoms based on patient-reported outcomes (PROs), by comparing assessments before and after treatment.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adult subjects between the ages of 19 and 75 years at the time of obtaining written informed consent. * Subjects who are scheduled to receive Fexuclu tablets (fexuprazan) in accordance with the approved indication. * Subjects who present with at least one subjective symptom requiring medical treatment * Subjects who are capable of understanding the information provided, have voluntarily decided to participate in this observational study, and have provided written informed consent for the use of their personal data. Exclusion Criteria: * Individuals who fall under any contraindications for the administration of Fexuclu tablets (fexuprazan) as specified in the approved labeling. * Individuals who are deemed by the investigator (attending physician) to be inappropriate for participation in this observational study for any reason not otherwise specified.
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What it tests

  • Not listed
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Where

1 site
Masong Kim Internal Medicine Clinic
Seoul, South Korea
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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