Clinical usefulness of high-sensitivity stool H. pyroli antigen test using BLEIA method

Clinical usefulness of high-sensitivity stool H. pyroli antigen test using BLEIA method - BLEIA study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000041890

Enrollment

220

Registered

2020-09-25

Start date

2020-10-01

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

H.Pylori infection

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Those who have been diagnosed as H. pirori positive and are planning eradication treatment

Exclusion criteria

Exclusion criteria: Penicillin allergy Postoperative upper gastrointestinal tract

Design outcomes

Primary

Measure	Time frame
Comparison for sensitivity of H. pylori stool antigen test (BLEIA method) with or without oral acid secretion inhibitor	—

Secondary

Measure	Time frame
Comparison of H. Pylori stool antigen test (BLEIA method) post-eradication accuracy with or without acid secretion inhibitor	—

Countries

Japan

Contacts

Public ContactChika Kusano

Department of Medicine, Nihon University School of Medicine Division of Gastroenterology and Hepatology, Department of Medicine

ckusano2007@yahoo.co.jp03-3293-1711

Outcome results