A RCT of Triple Therapy With Proton Pump Inhibitor vs Vonoprazan for Helicobacter Pylori Gastritis — TRIVON  

Helicobacter Pylori Infection Clinical Trial

Official title: A Randomized Controlled Trial of Triple Therapy With Conventional Proton Pump Inhibitor vs Triple Therapy With Vonoprazan as First Line Therapy for Helicobacter Pylori Gastritis

Status Recruiting

Clinical Trial Summary

Helicobacter pylori (H. pylori) gastritis is a common bacterial infection among the elderly population. H. pylori infection causes chronic progressive gastric inflammation, peptic ulcer disease and gastric cancer. Gastric cancer is a significant contributor of cancer-related mortality. The eradication of H. pylori reduces the incidence of gastric cancer. However, the efficacy of H. pylori eradication has decreased dramatically because of antibiotic resistance. This study aims to (i) compare the eradication rates of H. pylori by triple therapy with vonoprazan for the treatment of H. pylori gastritis) (TTV regimen), with triple therapy with conventional proton pump inhibitor (PPI) (TTP regimen) in a multi-racial Asian cohort, (ii) evaluate the prevalence of antibiotic (klacid/amoxicillin/levofloxacin/tetracycline) resistance in H. pylori infected patients, and (iii) assess the safety of the TTV regimen. Diagnosed H. pylori-infected patients (n=252) will be enrolled and randomized 1:1 to TTV or TTP regimen. Gastric biopsies will be cultured and antibiotic sensitivity evaluated using E-test/agar dilution method. The safety of TTV regimen will be assessed using adverse effect questionnaire. This study may potentially impact on prescribing policies and management of H. pylori infections for improved therapeutic outcome.

Clinical Trial Description

All subjects who present for endoscopy will be screened. Consent will be taken from subjects who are scheduled to undergo gastroscopy. Gastric biopsies to test for the presence of H. pylori using the rapid CLO test and for culture and sensitivity will be obtained. Based on an estimated prevalence of H. pylori of 20%, we aim to screen approximately 1000 subjects for H. pylori with the rapid CLO test during gastroscopy.

Subjects who have a negative CLO test during endoscopy will be excluded from the study and will be managed accordingly by their physician.

Subjects who are confirmed to have H. pylori gastritis based on the CLO test will then be recruited into the study.

Diagnosed H. pylori positive patients (n=252) will be enrolled into four study groups:

• Group A: Omeprazole 20mg bd/ Amoxicillin 1g bd/ Clarithromycin 500mg bd for 14 days

• Group B: Esomperazole 20mg bd/ Amoxicillin 1g bd/ Clarithromycin 500mg bd for 14 days

• Group C: Rabeprazole 20mg bd/ Amoxicillin 1g bd/ Clarithromycin 500mg bd for 14 days

• Group D: Vonoprazan 20mg bd/ Amoxicilllin 1g bd/ Clarithromycin 500mg bd for 7 days

Randomization codes will be generated by a computer program, and all codes are placed into sealed opaque envelopes and kept by an independent biostatistician. After obtaining informed consent, the investigators would call the research assistant to open the envelope for the allocated regimen. The allocation ratio for TTV and TTP groups is 1:1, with 126 patients in each group. Within the TTP group, the distribution of patients to each of the three PPIs (Omeprazole/Esomeprazole/Rabeprazole) will be equal (n=42 each). The compliance to treatment in terms of percentage of drugs taken will be assessed during clinic review.

This will be a single centre, prospective, open-label, randomized controlled study to (i) compare the eradication rates of H. pylori by TTP regimen vs TTV regimen in a multi-racial Asian cohort, (ii) evaluate the prevalence of antibiotic (clarithromycin/ amoxicillin/ levofloxacin/ tetracycline) resistance in H. pylori-infected patients of both treatment groups, and (iii) assess the safety of the TTV regimen. The proposed study workflow is outlined in Figure 1. This study will be conducted in CGH, in accordance with the ethical principles that have their origin in the Declaration of Helsinki, and are consistent with Good Clinical Practice, applicable regulatory requirements.

The demographic profile (age, gender, ethnicity) and clinical notes (endoscopic findings, antibiotic sensitivity testing results, drug regimen prescribed, extent of treatment compliance, duration of therapy, treatment outcomes i.e. eradication rate, occurrence of adverse events, etc.) of all patients enrolled into the study will be documented for data analysis.

The following experiments will be conducted for the study:

Efficacy assessment:

The success of treatment i.e. eradication of H. pylori is defined as a negative Carbon-13 urea breath test (CUBT) or negative histology test performed at week 6. CUBT or histology will be performed based on the clinical indication as determined by the attending physician. All patients should be off antibiotics and PPI or Vonoprazan for at least 4 weeks prior to assessment of the success of treatment, as per standard practice. All routine laboratory tests will be carried out in Microbiology Lab, Department of Laboratory Medicine, CGH. The technologists will be blinded to the treatment regimens.

Antibiotic susceptibility testing:

For patients with H. pylori infection diagnosed during endoscopy from a positive rapid urease test kit, the material from the test kit will be cultured for antibiotic sensitivity testing. The antibiotic sensitivity testing results may be of value in guiding the choice of antibiotics for second line salvage treatment should first line treatment fails. This has potential usage in the clinical management of patients.

Gastric biopsy specimens collected from both greater gastric corpus and antrum during endoscopy will be inoculated into H. pylori transport medium and transported with ice packs to the laboratory. The biopsy samples will be ground with a tissue homogenizer, cultured, followed by susceptibility testing and determination of the minimum inhibitory concentration (MIC). Briefly, culture will be performed with blood agar medium for Helicobacter with addition of 10% CO2 at 35°C for 7 days. The identity of H. pylori is defined as Gram-negative bacillus with catalase test positive, oxidase test positive, and urease test positive. The MIC of antibiotics (clarithromycin/ amoxicillin/ levofloxacin/ tetracycline) will be determined by E-test or agar plate dilution method in accordance with the guidelines established by the NCCLS Guidelines M100-S9. Mueller-Hinton agar (5% horse blood) will be used with addition of 10% CO2 at 35°C for 72 hours (21). The breakpoint for clarithromycin, amoxicillin, levofloxacin, and tetracycline resistance is defined as ≥ 1.0mg/L, 0.5mg/L, 1mg/L, and 1mg/L, respectively, according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) (21,22). The laboratory personnel involved in the antibiotic sensitivity testing will be blinded to the study group allocation.

Safety assessment:

An adverse effect questionnaire (AEQ) will be completed by all patients during therapy. The AEQ will contain a checklist to assess the occurrence of loose stools, skin eruption, abdominal bloating, constipation, nausea, epigastric pain, and dysgeusia.

Detection of mutational hotspots for clarithromycin resistance:

An in-house real-time PCR assay will be done on the DNA extracted from the cultured H. pylori isolates to detect mutational hotspots for clarithromycin-resistance.

Post-hoc CYP2C19 genotyping:

Genomic DNA will be extracted from peripheral leukocytes of whole blood using standard desalting methods. Genotyping for the two predominant single nucleotide polymorphisms (CYP2C19*2 and CYP2C19*3) leading to intermediate (heterozygous mutant) and poor metabolizer phenotypes (homozygous mutants) will be performed using sequencing of restriction fragment length polymorphism methods. ;

Related Conditions & MeSH terms

• Gastritis
• Helicobacter Pylori Infection

• NCT number: NCT03908619
• Study type: Interventional
• Source: Changi General Hospital
• Contact: Seok Hwee Koo, PhD
• Phone: 6568504929
• Email: seok_hwee_koo@cgh.com.sg
• Status: Recruiting
• Phase: Phase 4
• Start date: April 16, 2019
• Completion date: March 31, 2021