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ID06566898

Monitoring of Antimicrobial Resistance Based on Metagenomics Analyses in Pneumonia Patients: a Genomic Epidemiology Study

Led by Shanghai General Hospital, China · Updated on 2026-04-23

800

Participants Needed

1

Research Sites

24 weeks

Total Duration

On this page

Sponsors

S

Shanghai General Hospital, China

Lead Sponsor

W

Wuxi People's Hospital Affiliated to Nanjing Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying antimicrobial resistance (AMR) in patients with severe and mild pneumonia by analyzing their microbiomes using metagenomics. The study aims to understand the microbial communities present, the number of resistance genes carried by pathogens, and the genetic diversity of key pathogens from 2019 to 2025. This observational study collects data from multiple hospitals in China to improve pneumonia diagnosis and treatment strategies. Participants diagnosed with severe or mild pneumonia are identified based on established guidelines from the American Thoracic Society, Infectious Diseases Society of America, and British Thoracic Society. Clinical examination samples such as nasopharyngeal or oropharyngeal swabs, sputum, blood, lung tissue, and bronchoalveolar lavage fluid are collected. Advanced sequencing techniques, including next-generation sequencing on the Illumina Novaseq 6000 platform, are used to analyze the microbiome, viruses, bacteria, fungi, and antimicrobial resistance genes. Throughout the study period from 2019 to 2025, researchers analyze microbiome composition, alpha and beta diversity, and the presence of bacterial resistance genes. They use bioinformatics tools to filter and classify sequencing data, identify pathogens, and assess genetic diversity. Outcome measures focus on the microbiome's role in pneumonia, and findings will help characterize resistance patterns. The study runs until September 2026, with continuous recruitment and data collection.

CONDITIONS

Brief Title

Monitoring of Antimicrobial Resistance Based on Metagenomics Analyses in Pneumonia Patients

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients clinically diagnosed with severe or mild pneumonia according to ATS/IDSA 2019 guidelines for adults or BTS 2011 criteria for children
  • Clinical examination performed with available biological samples such as nasopharyngeal swab, oropharyngeal swab, bronchoalveolar lavage fluid, sputum, blood, hydrothorax, or lung tissue
Not Eligible

You will not qualify if you...

  • Patients whose biological samples may be contaminated
  • Patients with alveolar lavage fluid or hydrothorax volume less than 200 microliters

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 6 years (2019 to 2025)

Participants diagnosed with severe or mild pneumonia are observed to monitor antimicrobial resistance and microbiome composition through analysis of biological samples collected during routine clinical care.

Biological samples collected as part of clinical care during the study period

Trial Site Locations

Total: 1 location

1

Mei Kang

Shanghai, Shanghai Municipality, China, 200080

Actively Recruiting

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Research Team

M

Mei Kang, MPH

X

Xue Tian, Master

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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https://pubmed.ncbi.nlm.nih.gov/33069326

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https://pubmed.ncbi.nlm.nih.gov/33883479