← Back to Clinical Trials
Recruiting NCT07260006

NCT07260006 Treatment Efficacy of Regimens With and Without Bismuth in Children With Helicobacter Pylori-Associated Peptic Ulcer Disease

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07260006
Status Recruiting
Phase
Sponsor Can Tho University of Medicine and Pharmacy
Condition Helicobacter Pylori Infection
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2024-10-01
Primary Completion 2026-05-30

Eligibility & Interventions

Sex All sexes
Min Age 5 Years
Max Age 15 Years
Study Type INTERVENTIONAL
Interventions
Bismuth quadruple therapyTriple therapy with PPI + Amoxicillin + Metronidazole

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 80 participants in total. It began in 2024-10-01 with a primary completion date of 2026-05-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this clinical trial is to learn if including bismuth in the treatment helps heal stomach and duodenal ulcers caused by Helicobacter pylori (H. pylori) in children. The main questions it aims to answer are: * Does a treatment plan with bismuth work better than a plan without bismuth to clear the infection? * Is the bismuth plan more cost-effective while still safe and effective? Researchers will compare two treatment groups to see which works better. Participants will: * Take one of the two assigned treatment plans (with or without bismuth) for the standard treatment duration * Visit the clinic for checkups and tests to confirm infection clearance and monitor side effects * Keep a diary of symptoms, medication use, and any side effects

Eligibility Criteria

Inclusion Criteria: * Diagnosed with gastritis or peptic ulcer disease by upper gastrointestinal endoscopy or histopathology. * Meets diagnostic criteria for Helicobacter pylori infection. * Parent or legal guardian provides consent for the child to participate in the study. Exclusion Criteria: * Allergic to any of the medications in the treatment regimen. * Use of antibiotics or bismuth within the past 4 weeks, or use of antacids, H2-receptor antagonists, or proton pump inhibitors within the past 2 weeks. * Failure to return for follow-up visits after treatment.

Contact & Investigator

Central Contact

Trang Thuy Mai, MD

✉ maithuytrang2000@gmail.com

📞 +84 838 857 890

Frequently Asked Questions

Who can join the NCT07260006 clinical trial?

This trial is open to participants of all sexes, aged 5 Years or older, up to 15 Years, studying Helicobacter Pylori Infection. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07260006 currently recruiting?

Yes, NCT07260006 is actively recruiting participants. Contact the research team at maithuytrang2000@gmail.com for enrollment information.

Where is the NCT07260006 trial being conducted?

This trial is being conducted at Can Tho, Vietnam.

Who is sponsoring the NCT07260006 clinical trial?

NCT07260006 is sponsored by Can Tho University of Medicine and Pharmacy. The trial plans to enroll 80 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology