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Comparison of standard anti-Helicobacter pylori eradication regimen with and without N Acetylcysteine ??in patients with dyspepsia

Comparison of standard anti-Helicobacter pylori eradication regimen with and without N Acetylcysteine ??in patients with dyspepsia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201078634N1
Enrollment
100
Registered
2012-05-07
Start date
2012-01-20
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

Dyspepsia. Helicobacter pylori [H.pylori] as the cause of diseases classified

Interventions

Intervention 1: Intervention group received standard treatment of anti H pylori which include Amoxicillin 500 mg four times daily, Bismuth citrate 120 mg four times daily, Omeprazole 20 mg twice dai
Treatment - Drugs
Intervention group received standard treatment of anti H pylori which include Amoxicillin 500 mg four times daily, Bismuth citrate 120 mg four times daily, Omeprazole 20 mg twice daily, Clarithromyc
Control group received standard treatment of anti H pylori which include Amoxicillin 500 mg four times daily, Bismuth citrate 120 mg four times daily, Omeprazole 20 mg twice daily, Clarithromycin 500

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included: All patients with gastrointestinal symptoms and dyspepsia which refer to the Gastroenterology Clinics of Al-Zahra hospital, Noor, Poursina Hakim Research Center and Ardakan hospital for endoscopy by a gastroenterologist recruited with full consent if Helicobacter pylori tests were positive (confirmed by histology, Rapid urease test or stool antigen test). Exclusion criteria included: Patients previously received eradication of Helicobacter pylori treatment? Presence of underlying disease such as cirrhosis? Renal failure? Severe cardiac disease? malignancy outside of the GI? Age less than 17 and more than 80? Simultaneous use of NSAIDs? Concomitant use of steroids? Recent gastrointestinal bleeding? pregnancy or lactation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication. Timepoint: Prior to and one month after intervention. Method of measurement: Stool antigen.

Secondary

MeasureTime frame
Drug side effects. Timepoint: During and after drug consumption. Method of measurement: Visiting and call-chek list.;Drug tolerance. Timepoint: During drug consumption. Method of measurement: Visiting and call.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehdi Zobeiri

Kermanshah University of Medical Sciences

mzoberi@kums.ac.ir; mehdizobeiri@yahoo.com+98 31 1624 9030

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 19, 2026