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Clinical Trials/NCT06274931
NCT06274931
Recruiting
Not Applicable

Analysis of the Pulmonary Microbiome

University Magna Graecia1 site in 1 country30 target enrollmentFebruary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pneumonia
Sponsor
University Magna Graecia
Enrollment
30
Locations
1
Primary Endpoint
Assessment of Lung Microbiome in Acute Respiratory Failure
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of the protocol is to study the pulmonary microbiome in patients who develop pneumonia.

Detailed Description

The purpose of the protocol is to study the pulmonary microbiome in patients who develop pneumonia with severe acute respiratory failure, requiring admission to the Intensive Care Unit, and to compare it with that of patients diagnosed with pneumonia but who do not develop severe acute respiratory failure and subsequent admission to the intensive care unit.

Registry
clinicaltrials.gov
Start Date
February 1, 2024
End Date
June 20, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Magna Graecia
Responsible Party
Principal Investigator
Principal Investigator

Andrea Bruni

Professor

University Magna Graecia

Eligibility Criteria

Inclusion Criteria

  • Patients with acute respiratory failure
  • Patients with suspect of pneumonia

Exclusion Criteria

  • pregnancy
  • age \< 18 years

Outcomes

Primary Outcomes

Assessment of Lung Microbiome in Acute Respiratory Failure

Time Frame: The study will be conducted over a period of two months, during which data collection, bronchoscopic examinations, and analysis of the lung microbiome will be carried out.

This study aims to investigate the composition and diversity of the lung microbiome in patients experiencing acute respiratory failure. Specifically, the research evaluates differences in the lung microbiome between ICU-admitted patients, non-hospitalized individuals, and a control group without known lung pathologies. Through bronchoscopic examinations and alveolar bronchial lavage, the study seeks to elucidate potential associations between lung microbiota and the development of acute respiratory failure. For the analysis of the lung microbiome, the MiSeq Reagent Nano v2 kit is utilized. This kit enables high-throughput sequencing of microbial DNA extracted from samples obtained via bronchoscopic examinations and alveolar bronchial lavage. The MiSeq platform provides accurate and comprehensive data on the microbial composition and diversity present in the lung microbiome of study participants.

Study Sites (1)

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