Rheumatoid arthritis (RA) NSAIDs-induced gastrointestinal mucosal injury
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. RA patients receiving traditional NSAIDs for twelve or more month 2. Patients of 20 years or more regardless of their gender, or being outpatients or not 3. Patients giving informed consent
Exclusion criteria
Exclusion criteria: Patients with 1. Gastrectomy or vagotomy 2. Malignancy 3. Severe hepatic dysfunction 4. Severe renal dysfunction 5. Severe cardiac dysfunction 6. hematologic disease 7. Patients showing hypersensitive reaction to celecoxib or one member of the sulfonamide class 8. Patients being pregnant or plan to become pregnant during treatment 9. Patients who are regarded as inadequate subject by physician in charge
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in incidence of gastroduodenal mucosal injury. | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of gastroduodenal mucosal injury in patients with long-term NSAIDs therapy Changes in disease activity measures of rheumatoid arthritis after switching to celecoxib Adverse side effect | — |
Countries
Japan
Contacts
Hoshigaoka Koseinenkin Hospital Dept. of Clinical Trial Management