Status: Not yet recruiting
Fexuclue for Prevention of NSAIDs-Induced Peptic Ulcer in Real-World Practice
This study is a prospective, multi-center, observational study to evaluate the efficacy and safety of Fexuclue Tablet 20 mg in patients requiring prevention of NSAIDs-induced peptic ulcer in real-world clinical practice in Korea. Patients receiving NSAIDs and requiring gastroprotective therapy will be enrolled and followed prospectively. The study will assess patient-reported outcomes (PROs) related to gastrointestinal symptoms, as well as safety outcomes.
Participants needed: 7,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Daewoong Pharmaceutical Co. LTD.Updated: Apr 30, 2026Locations: 1
Eligibility criteria
Adults aged ≥19 years [+4]
Hypersensitivity to Fexuclue or its components [+3]