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Efficacy of Proton Pump Inhibitors in Gastrointestinal Erosions and/or Ulcers

S

Shinshu University

Status and phase

Enrolling
Phase 2

Conditions

Gastrointestinal Erosions and/or Ulcers

Treatments

Drug: Oral Esomeprazol
Drug: Oral Bonoprazan

Study type

Interventional

Funder types

Other

Identifiers

NCT03315676
PPI 2017

Details and patient eligibility

About

The aim of this study is to collect the data of clinical efficacy and safety after the usage of bonoprazon and esomeprazole when the patients take NSAIDs more than 2 weeks and have gastrointestinal symptoms who have had gastrointestinal erosions and/or ulcers in the past.

Enrollment

124 estimated patients

Sex

All

Ages

20 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of NSAIDs-induced gastrointestinal Erosions and/or Ulcers who want to take Bonoprazan or Esomeprazole

Exclusion criteria

  • Patients allergic to Bonoprazan or Esomeprazole

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

124 participants in 2 patient groups

Oral Bonoprazan
Active Comparator group
Description:
Daily intake of Bonoprazan
Treatment:
Drug: Oral Bonoprazan
Oral Esomeprazol
Active Comparator group
Description:
Daily intake of Esomeprazol
Treatment:
Drug: Oral Esomeprazol

Trial contacts and locations

1

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Central trial contact

Yukio Nakamura, MD, PhD

Data sourced from clinicaltrials.gov

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