The Utility of Rapid Urine Test in the Diagnosis of Helicobacter pylori infection in Patients with Non-Variceal Upper Gastrointestinal Hemorrhage

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20250302002

Enrollment

120

Registered

2025-03-02

Start date

2024-07-01

Completion date

Unknown

Last updated

2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

the sensitivity and specificity of Urine rapid antibody test in non-variceal upper GI bleeding patients. Rapid urine test

Interventions

Collect patient urine and test the urine.

No Intervention No treatment

Rapid urine test

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. The subject is more than 18 years old and was diagnosed with non-variceal upper gastrointestinal bleeding at Bhumibol Adueyadej Hospital.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to any of the diagnostic modalities being employed. 2. Individuals who have received eradication treatment for Helicobacter pylori within the 12 months preceding their enrollment in the study. 3. Individuals who are unable or unwilling to provide informed consent.

Design outcomes

Primary

Measure	Time frame
Urine rapid test at event positive test	—

Secondary

Measure	Time frame
N/A N/A N/A	—

Countries

Thailand

Contacts

Public ContactChanunta HONGTHANAKORN

Bhumibol Adueyadej Hospital

rabbithap@yahoo.com665437000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026