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Comparison of Sequential therapy with standard therapy for eradication of H.Pylori infection in uremic patients

Comparison of Sequential therapy with standard therapy for eradication of H.Pylori infection in uremic patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138706211241N1
Enrollment
40
Registered
2009-07-15
Start date
2009-08-23
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

H. Pylori infection. Other specified bacterial agents as the cause of diseases classified to other chapters

Interventions

Intervention 1: Intrvention group: seqential treatment:Pantoprazole (40mg BD) Amoxicillin (if clearances of cratinin is between 3-10 mg/dl 250-500 mg BD and if it is lower 10mg/dl 250-500 mg Daily, (f
Treatment - Drugs
Intrvention group: seqential treatment:Pantoprazole (40mg BD) Amoxicillin (if clearances of cratinin is between 3-10 mg/dl 250-500 mg BD and if it is lower 10mg/dl 250-500 mg Daily, (for the first fiv
Control group: Standard regimen: Amoxicillin (if clearances of cratinine is between 3-10 mg/dl 250-500 mg BD and if it is lower 10mg/dl 250-500 mg Daily), Pantoprazole (40 mg BD) and Claithromycin (25

Sponsors

Mazandaran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age more than 18 years, dyspepsia during last month and positive H.pylori infection (positive rapid urease test and positive biopsy by endoscope). Exclusion criteria: Antibiotic therapy for eradication of H.pylori, consumption of Proton Pump Inhibitor, H2 blockers, Bismuth, or NSAIDS during last month, consumption of anticoagulants, Ketoconazol or corticosteroids, history of gastric or esophageal surgery, hypersensitivity to antibiotics, negative biopsy of GI, smoking or alcohol use, pregnancy, lactation, severe heart diseases (MI, EF = 30), liver & thyroid diseases and malignancy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Eradication of H. Pylori infection. Timepoint: 3 month after treatment. Method of measurement: Stool antigen test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtieh Makhlough

Mazandaran Univercity of Medical Sciences and Health Services

makhlough_a@yahoo.com+98 15 1226 1700

Outcome results

None listed

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