Skip to content

Evaluation of the diagnosis accuracy and eradication protocol of Helicobacter pylori gastritis in CKD 5 hemodialysis patients

Evaluation of the diagnosis accuracy and eradication protocol of Helicobacter pylori gastritis in CKD 5 hemodialysis patients - The diagnosis and eradication of Helicobacter pylori in CKD

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000013660
Enrollment
30
Registered
2014-04-08
Start date
2014-04-08
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

Hemodialysis patients with Helicobacter pylori gastritis

Interventions

None listed

Sponsors

Division of Clinical Nephrology & Rheumatology, Niigata University Graduate School of Medical & Dental Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients of CKD stage G4 ~ 5 (eGFR <= 30, including hemodialysis patients 2) Patients were revealed as chronic gastritis by upper gastrointestinal fiberscopy 2) Outpatients with relatively stable renal function. 3) Patients who can take medication orally. 4) Patients who can receive blood tests. 5) Patients that agreed to diagnosis and treatment of H.pyroli. 6) Men and women aged over 20 years old

Exclusion criteria

Exclusion criteria: 1) Patients with a history of hypersensitivity for amoxicillin, clarithromycin, proton pump inhibitors, or metronidazole. 2) Of the patients with CKD, the patient being predicted for initiating dialysis within six months. 3) Patients complicated with acute inflammatory disease or active infection. 4) Patients with active malignant tumor. 5) Patients who suspected of being pregnant or pregnancy. 6) Patients did not make a consent for test and/or treatment of H. pyroli gastritis. 7) Patients was determined to be difficult to continue the eradication therapy by serious adverse events. 8) Patients offer discontinuation of the study. 9) Attending physician deems the patients as unsuitable of the study.

Design outcomes

Primary

MeasureTime frame
Eradication rate for Helicobacter pyroli

Secondary

MeasureTime frame
Sensitivity and specificity of anti-Helicobacter pylori Antibody-IgG, Dry weight during dialysis, blood pressure, body weight, chest X-ray CTR, hemoglobin, dose of ESA, serum iron, UIBC (not to TIBC), ferritin, CRP.

Countries

Japan

Contacts

Public ContactYuichi SAKAMAKI

Niigata University Graduate School of Medical & Dental Sciences Division of Clinical Nephrology & Rheumatology

ysakamaki-dm@umin.net+81-25-227-2200

Outcome results

None listed

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