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Post-Marketing Surveillance of Acofide in Patients with Functional Dyspepsia

Post-Marketing Surveillance of Acofide in Patients with Functional Dyspepsia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080222794
Enrollment
3000
Registered
2015-02-13
Start date
2015-02-13
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

Functional Dyspepsia

Interventions

investigational material(s) Generic name etc : Acofide tablets 100mg INN of investigational material : Acotiamide Therapeutic category code : 239 Other agents affecting digestive organs Dosage and Adm

Sponsors

ZERIA Pharmaceutical Co.,Ltd.
Lead Sponsor
Astellas Pharma Inc.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: postprandial fullness, upper abdominal bloating, early satiety

Exclusion criteria

Exclusion criteria: malignant disease in upper gastrointestinal tract

Design outcomes

Primary

MeasureTime frame
Safety rate of side effects

Secondary

MeasureTime frame
efficacy improvement rate

Outcome results

None listed

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