Actively Recruiting
Monitoring of Antimicrobial Resistance Based on Metagenomics Analyses in Pneumonia Patients
Led by Shanghai General Hospital, China · Updated on 2026-04-23
800
Participants Needed
1
Research Sites
112 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
Monitoring of antimicrobial resistance (AMR) based on metagenomics analyses in pneumonia patients is critical for optimizing clinical diagnosis and treatment and improving clinical prognosis. This study is designed to ask the following key questions: 1. What is the microbiome maps of patients with severe pneumonia and mild pneumonia ? 2. How many pathogen resistance genes are carrying in severe pneumonia and mild pneumonia ? 3. What is the genetic diversity of key pathogens detected in severe pneumonia and mild pneumonia during 2019-2025?
CONDITIONS
Official Title
Monitoring of Antimicrobial Resistance Based on Metagenomics Analyses in Pneumonia Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients clinically diagnosed with severe or mild pneumonia according to ATS/IDSA guidelines for adults or BTS guidelines for children
- Diagnosis based on meeting at least one major or three minor criteria as defined in these guidelines
- Clinical examination performed with remaining biospecimens such as nasopharyngeal swabs, oropharyngeal swabs, bronchoalveolar lavage fluid, sputum, blood, hydrothorax, or lung tissue from microbiological testing
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mei Kang
Shanghai, Shanghai Municipality, China, 200080
Actively Recruiting
Research Team
M
Mei Kang, MPH
CONTACT
X
Xue Tian, Master
CONTACT
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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