MedPath

Helicobacter Pylori 23S rRNA/gyrA Gene Mutation Detection Kit (Fluorescence PCR Fusion Curve Method)

Completed
Conditions
Fecal Drug Resistance Gene Detection
Helicobacter Pylori Infection, Susceptibility to
Helicobacter Pylori gyrA Levofloxacin Resistance Mutation
Helicobacter Pylori Infection
Interventions
Diagnostic Test: Sanger Sequencing group
Diagnostic Test: Bacterial culture and drug sensitivity test of gastric mucosa samples
Diagnostic Test: Detection of fecal samples with diagnostic kit
Registration Number
NCT05410652
Lead Sponsor
Nanjing First Hospital, Nanjing Medical University
Brief Summary

The purpose of this study was to evaluate the detection ability of Helicobacter pylori 23S rRNA/gyrA gene mutation detection kit (fluorescent PCR fusion curve method) for Helicobacter pylori gene mutation.

Detailed Description

After being informed about the study and potential risks, all patients giving written informed consent will undergo a 1-week screening period to determine eligibility for study entry. At week 0, patients who meet the eligibility requriment will be included in this simultaneous blind test.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1176
Inclusion Criteria
    1. patients with Helicobacter pylori infection who need gastroscopy; 2. patients with positive Helicobacter pylori culture in gastric mucosa 3. Helicobacter pylori negative patients
Exclusion Criteria
  • 1.Patients with insufficient fecal samples collected 2.Patients with contraindication of gastroscopic biopsy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Sanger Sequencing groupSanger Sequencing groupDetection of gyrA and 23S rRNA mutations in H. pylori isolated from Gastric Mucosa by Sanger Sequencing
Drug sensitivity test groupBacterial culture and drug sensitivity test of gastric mucosa samplesGastroscopy was performed on patients who met the inclusion and exclusion criteria to obtain samples of gastric mucosa. Helicobacter pylori culture and drug sensitivity test were performed on gastric mucosa samples in vitro. Finally, the drug sensitivity test results were collected.
Fecal kit groupDetection of fecal samples with diagnostic kitCollect stool samples from patients who meet the inclusion criteria. DNA was extracted from fecal samples. After that, the extracted DNA was sequenced by first generation sequencing. Finally,the mutation sites of extracted DNA were detected by fecal gene detection kit.
Primary Outcome Measures
NameTimeMethod
Evaluation of consistency between fecal gene detection kit and first generation sequencing4 weeks

Compare the positive coincidence rate, negative coincidence rate, total coincidence rate and consistency between stool gene detection kit and first generation sequencing

Evaluation of consistency between fecal gene detection kit and Drug sensitivity test4 weeks

Compare the positive coincidence rate, negative coincidence rate, total coincidence rate and consistency between stool gene detection kit and drug sensitivity test

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

The First Affiliated Hospital of Zhejiang Chinese Medical University

🇨🇳

Hangzhou, Zhejiang, China

Jiangsu Taizhou People's Hospital

🇨🇳

Taizhou, Jiangsu, China

The First Affiliated Hospital of Nanchang University

🇨🇳

Nanchang, Jiangxi, China

Nanjing First Hospital, Nanjing Medical University

🇨🇳

Nanjing, Jiangsu, China

© Copyright 2025. All Rights Reserved by MedPath