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Rabeprazole specific clinical experience investigation for the long-term combination therapy with low-dose aspirin

Rabeprazole specific clinical experience investigation for the long-term combination therapy with low-dose aspirin

Status
Unknown
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080222833
Enrollment
1400
Registered
2015-04-27
Start date
2015-04-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gastric ulcer, Duodenal ulcer

Interventions

investigational material(s) Generic name etc : Pariet INN of investigational material : Rabeprazole Sodium Therapeutic category code : 232 Agents for peptic ulcer Dosage and Administration for Investi

Sponsors

Eisai Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients taking long-term low-dose aspirin for prevention of thrombus/embolism at the start of administration of rabeprazole(including patients who start low-dose aspirin on the same day as the start of administration of rabeprazole) (2)Patients with a history of gastric/duodenal ulcers (3)Patients requiring long-term use of rabeprazole for prevention of recurrence of gastric/duodenal ulcers induced by low-dose aspirin

Exclusion criteria

Exclusion criteria: (1)Patients with gastric/duodenal ulcers at the start of administration of rabeprazole (2)Patients with active upper gastrointestinal bleeding at the start of administration of rabeprazole (3)Patients with contraindication for rabeprazole

Design outcomes

Primary

MeasureTime frame
Incidence of adverse drug reactions Confirm of adverse drug reactions

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026