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Assessment of efficacy of N-Acetylecysteine plus standard quadruple therapy regimen in comparison to standard quadruple therapy regimen for H. pylori infection eradiacation

Assessment of efficacy of N-Acetylecysteine plus standard quadruple therapy regimen in comparison to standard quadruple therapy regimen for H. pylori infection eradiacation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201605201155N24
Enrollment
46
Registered
2016-08-30
Start date
2016-08-22
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. Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters

Interventions

Intervention 1: The experimental group was given amoxicillin (capsules, 1000?mg) bid (with breakfast and dinner), clarithromycin (capsules, 500?mg) bid (with breakfast and dinner), and omeprazole (cap
Treatment - Drugs
The experimental group was given amoxicillin (capsules, 1000?mg) bid (with breakfast and dinner), clarithromycin (capsules, 500?mg) bid (with breakfast and dinner), and omeprazole (capsules, 20?mg) bi
(The control group was given amoxicillin/clarithromycin/omeprazole the same as experimental group, plus placebo.In patients without peptic ulcer, omeprazole 20?mg once daily was continued for 2 weeks.

Sponsors

Vice chancellor for research of Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with peptic-like epigastric pain and dyspeptic symptoms, referred to the endoscopy unit and scheduled for upper GI endoscopy and with positive rapid urease test Exclusion criteria: age70, recent use of antibiotics, bismuth salts, or proton pump inhibitors (PPI), chronic use of nonsteroidal anti-inflammatory drugs or corticosteroids, gastric outlet obstruction, pregnancy, renal failure, gastric malignancy, and prior gastric surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Eradocation of Helicobacter pylori. Timepoint: before initiate Intervention, two wk after finishing the intervention. Method of measurement: Urease breath test.

Secondary

MeasureTime frame
Side effects. Timepoint: before initiating intervention, 2 wk after finishing the intervention. Method of measurement: physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarahnaz Joukar

Gastrointestinal and Liver Disease Research Center(GLDRC)

F_Jokar@gums.ac.ir+98 13133535116

Outcome results

None listed

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