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Comparison of acid inhibition attained by Vonoprazan with or without Lafutidine.

Comparison of acid inhibition attained by Vonoprazan with or without Lafutidine. - Comparison of acid inhibition attained by Vonoprazan with or without Lafutidine.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022290
Enrollment
30
Registered
2016-07-01
Start date
2016-07-01
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

Reflux esophagitis

Interventions

There are three regimens as follows
(1) Vonoprazan 20mg once daily for 7 days, (2) Vonoprazan 10mg once daily for 7 days, (3) Vonoprazan 10mg and Lafutidine 10mg once daily for 7 days. Subujects receive the three different regimens in a
regimen (1), washout (at least 2 weeks), regimen (2), washout (at least 2 weeks), and regimen (3). Interventions 2
regimen (1), washout (at least 2 weeks), regimen (3), washout (at least 2 weeks), and regimen (2). Interventions 3
regimen (2), washout (at least 2 weeks), regimen (1), washout (at least 2 weeks), and regimen (3). Interventions 4
regimen (2), washout (at least 2 weeks), regimen (3), washout (at least 2 weeks), and regimen (1). Interventions 5
regimen (3), washout (at least 2 weeks), regimen (1), washout (at least 2 weeks), and regimen (2). Interventions 6
regimen (3), washout (at least 2 weeks), regimen (2), washout (at least 2 weeks), and regimen (1).

Sponsors

First Department of Medicine and Center for Clinical Research, Hamamatsu University School of Medicine, Hamamatsu, Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy Japanese men and women.

Exclusion criteria

Exclusion criteria: Exclusion criteria are any underlying disease, smoking habit, past or present H.pylori infection, and habitual use of any medicine.

Design outcomes

Primary

MeasureTime frame
The primary outcome is acid inhibition with the three regimens as assessed by 24-hour intragastric pH monitoring on Day7 in each regimen.

Countries

Japan

Contacts

Public ContactTakahisa Furuta

Hamamatsu University School of Medicine Center for Clinical Research

furuta@hama-med.ac.jp053-435-2261

Outcome results

None listed

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