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study of effect of H2RA for the epigastric symptoms

study of effect of H2RA for the epigastric symptoms - study of effect of H2RA for the epigastric symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004769
Enrollment
30
Registered
2011-12-22
Start date
2011-02-01
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 and gastroesophageal reflux diseases

Interventions

Roxatidine 75mg

Sponsors

Gastroenterology Division, Yokohama City University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient with epigastric symptoms before endoscopy.

Exclusion criteria

Exclusion criteria: 1)Patient who has ulcer [**] 2)Patient who receives operation of gut excision and vagectomy 3)Patient who has diseases of serious renal damage, hepatic toxicit, and blood trouble, etc. 4)Patient who has malignant tumor 5)Patient who has possibility of pregnant woman and pregnancy 6)Patient who has change in dosage taking NSAID and gut movement activating medicine, and before and after experimental drug taking 7)Patient who is administering antsecratory medcines such as PPI and H2RA (H2RA needs the doing taking medicine period for PPI for two weeks or more for one week or more for the patient who had been administered before. ) 8)Patient who has allergic history for experimental roxatidine 9)Patient who assumes judgment from doctor when it is improper as object of this study

Design outcomes

Primary

MeasureTime frame
epigastric symptoms

Countries

Japan

Contacts

Public ContactMasahiko Inamori

Yokohama City University Graduate School of Medicine Gastroenterology Division

inamorim@med.yokohama-cu.ac.jp045-787-2640

Outcome results

None listed

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