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Comparison of Sequential therapy for eradication of H. Pylori infection in renal failure patients

Comparison of Sequential therapy for eradication of H. Pylori infection in renal failure patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201231241N3
Enrollment
80
Registered
2012-03-01
Start date
2010-09-11
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Helicobacter pylori infection. Helicobacter pylori

Interventions

Intervention 1: Intervention Group:Pantoprazul (BD40mg) and amoxicillin (If keratinize clearance is between 10-30:250-500mg BD and if it is less than 10:250-500 mg Daily)for 5 days and Then Pantopraz
Treatment - Drugs
Intervention Group:Pantoprazul (BD40mg) and amoxicillin (If keratinize clearance is between 10-30:250-500mg BD and if it is less than 10:250-500 mg Daily)for 5 days and Then Pantoprazul (40mg BD) and
Control Group : Pantoprazul (40mg BD) and Claritromicine(250 mg BD)and Amoxicillin (If Kratinize Cearance is between 10-30:250-500mg BD and if it is less than 10:250-500 mg Daily)

Sponsors

Department of Research and Technology, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with dyspepsia symptoms over the past one month from gastroenterology or nephrology clinic or hospital dialysis ward who have infection with H. Pylori confirmed by rapid urease test and biopsy in endoscopy. Exclusion Criteria : taking antibiotic regimen to eradicate H. pyloriand or receiving proton pump inhibitors, Bismuth, or NSAID during the last month; concomitant anticoagulant, corticosteroid or Ketoconazole; history of gastric or esophageal surgery; sensitivity to antibiotics; negative endoscopic biopsy; drinking alcohol and smoking; pregnancy and lactation; severe heart disease; diseases of the thyroid gland or liver cancer; chronic renal failure patients who are prior to stage 5 or have not received renal replacement therapy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Eradication of Helicobacter pylori Infection. Timepoint: At the end of four weeks after treatment. Method of measurement: Urea Test.;Eradication of Helicobacter pylori Infection. Timepoint: At the end of four weeks after treatment. Method of measurement: Creatinine Clearance Test.;Eradication of Helicobacter pylori Infection. Timepoint: At the end of four weeks after treatment. Method of measurement: Stool examination.;Eradication of Helicobacter pylori Infection. Timepoint: At the end of four weeks after treatment. Method of measurement: Biopsy by Endoscopic.

Secondary

MeasureTime frame
Acute Renal Failure. Timepoint: At the first and second weeks of treatment. Method of measurement: Testing Urea.;Acute Renal Failure. Timepoint: At the first and second weeks of Treatment. Method of measurement: creatinine clearance test.;Acute Renal Failure. Timepoint: at the first and second weeks of treatment. Method of measurement: weight.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Atieh Makhlough

Mazandaran University of Medical Sciences

dr.makhloogh@mazums.ac.ir , makhlough_a@yahoo.com+98 15 1226 4047

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026