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Role of Vonaprazan in H.Pylori eradication

Comparison of efficacy and safety of 7-days vonoprazan versus 14-days esomeprazole based triple therapy for H- pylori infection

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221207056738N1
Enrollment
122
Registered
2022-12-28
Start date
2022-12-20
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Helicobacter pylori infection is a condition in which gram -ve bacteria called H- pylori reside in mucus lining of stomach lead to gastritis, ulcer manifest in the form of dyspepsia. Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere

Interventions

Intervention 1: Intervention group: group 2 is the interventional group to which 7-days vonoprazan based triple therapy, new drug regimen, vonoprazn 20mg BD, amoxicillin 1000mg BD, levofloxacin 500mg

Sponsors

National university of Medical Sciences Rawalpindi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Positive stool antigen test for h-pylori,endoscopic histopathological evidence of h-pylori. Age 18 years and above Both male and female patients presented with symptoms of dyspeps

Exclusion criteria

Exclusion criteria: Patient with history of drug allergy to either Pantoprazole, Vonoprazan Vonoprazan, penicillin’s or clarithromycin , Previous h-pylori eradication therapy, Pregnant and breast-feeding mothers, Patient with serious CVS, liver, renal, pulmonary disorders or acute malignancy, ,History of gastric malignancy or surgery, History of drug abuse. History of using anti-biotics that affect h-pylori with in 4 weeks

Design outcomes

Primary

MeasureTime frame
Conversion of stool antigen from positive to negative. Timepoint: After 4 weeks after the therapy. Method of measurement: Lab investigation. clinical assessment for symptoms improvement and side effects.

Secondary

MeasureTime frame
Improvement of clinical symptoms, side effects ,drug compliance,tolerability. Timepoint: 2 and 4 weeks after intervention. Method of measurement: Through telephone and after 4 weeks at hospital OPD.

Countries

Pakistan

Contacts

Public ContactFarzana Waqar

National University of Medical Sciences Rawalpindi

drfaru11@gmail.com+92 51 4251022

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026