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

NCT06948487 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 12000

Last updated 2025-07-17

No results posted yet for this study

Summary

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.

Conditions

  • Gastritis

Sponsors & Collaborators

  • Daewoong Pharmaceutical Co. LTD.

    lead INDUSTRY

Principal Investigators

  • Jingun Kim, Dr. · Masong Kim Internal Medicine Clinic

Eligibility

Min Age
19 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-17
Primary Completion
2025-11-30
Completion
2027-06-03

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06948487 on ClinicalTrials.gov