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Effect of helicobacter pylori eradication regimen versus standard treatment on gastro-esophageal reflux symptoms in patients with antral gastritis

Effect of helicobacter pylori eradication regimen versus standard treatment on gastro-esophageal reflux symptoms in patients with antral gastritis: a triple blinded randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202229014N2
Enrollment
162
Registered
2012-05-28
Start date
2012-05-21
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

Gastroesophageal reflux. Gastro-oesophageal reflux disease without oesophagitis

Interventions

Intervention 1: Intervention group will receive eradication treatment including Omeprazole 20 mg BID, Clarithromycin 500 mg BID, and Amoxicillin 1000 mg BID for two weeks. Intervention 2: Control grou
Treatment - Drugs
Intervention group will receive eradication treatment including Omeprazole 20 mg BID, Clarithromycin 500 mg BID, and Amoxicillin 1000 mg BID for two weeks
Control group will receive standard treatment for reflux including Omeprazole 20 mg BID for two weeks

Sponsors

Vic-chancellor of Research and Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient's with one of the following symptoms: gastro-esophageal reflux, dysphagia; heartburn; nausea; chest pain; and nuisance conditions that lead to awakening the patient will be included if they have endoscopic detection of gastritis and H. pylori infection in biopsy of gastric mucosa. The patents with following characteristics will be excluded from the study: simultaneous gastritis of fundus and antrum (pangastritis); gastric ulcer; duodenal ulcer; surgical history of esophagus, stomach, or duodenum; and history of using NSAIDs.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency and severity of reflux. Timepoint: After four weeks. Method of measurement: History taking of heartburn, regurgitation, nausea, dysphagia, chest pain, and nocturnal.

Secondary

MeasureTime frame
Abdominal pain and diarrhea. Timepoint: Two weeks later. Method of measurement: History taking.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Jalal Poorolajal

Research Center for Health Sciences and Department of Epidemiology & Biostatistics

poorolajal@umsha.ac.ir+98 81 1838 0090

Outcome results

None listed

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