Clinical Trials Directory

Trials / Unknown

UnknownNCT03397680

Effectiveness of Once-daily Dose Regimen of 7-day and 14-day High Dose Rabeprazole-levofloxacin Based Quadruple Therapy for H. Pylori Eradication in Thai Patients With Non-ulcer Dyspepsia

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Thammasat University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

H.pylori is an organism which causes gastric inflammation, peptic ulcer disease (PUD), mucosa associated lymphoid tissue (MALT) lymphoma and gastric cancer. Practical guideline for treatment of patients with dyspepsia and H.pylori eradication recommended the 14-day triple therapy regimen which had curable about 70% by using proton pump inhibitor (PPI) combined with antibiotics including amoxicillin, clarithromycin and metronidazole. Up to date, there has been no evidence about the cure rate for H.pylori eradication with once-daily dose regimen of high dose rabeprazole and levofloxacin based therapy. This research is to study the 7-day and 14-day cure rate of H.pylori eradication treatment with once-daily regimen of high dose rabeprazole-levofloxacin based quadruple therapy.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TEST13C Urea Breath TestAfter the H.pylori eradication treatment course completed, participants then was tested with 13C Urea Breath Test to confirm treatment effectiveness at least after ceasing PPI and antibiotics for 4 weeks.

Timeline

Start date
2017-05-15
Primary completion
2018-05-15
Completion
2018-05-15
First posted
2018-01-12
Last updated
2018-05-01

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT03397680. Inclusion in this directory is not an endorsement.