Pathogenic Microorganisms in Adult Severe Pneumonia Patients

NCT ID: NCT04433403

Last Updated: 2021-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-07-01

Study Completion Date

2024-06-30

Brief Summary

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This study aimed to evaluate pathogenic microorganisms in adult severe pneumonia patients in different cities of Liaoning Province

Detailed Description

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The pathogenic microorganisms of adult patients with severe pneumonia is detected in this study. Clinical treatment does not involve , so it meets the ethical requirements. The clinical data, laboratory test results and imaging data of adult severe pneumonia patients in different hospitals in different cities are recorded. The pathogenic microorganism is detected by second-generation sequencing of lower respiratory tract sputum or alveolar lavage fluid samples, and the data were sorted out to draw the pathogenic microorganism spectrum of adult severe pneumonia in Liaoning area. It will be used to guide clinical empirical treatment.

Conditions

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Pathogenic Microorganism of Serious Pneumonia

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

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pathogenic microorganism

Detection of pathogenic microorganisms in adult severe pneumonia by second generation sequencing

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Meet the standard of severe pneumonia: Main standards: Requiring mechanical ventilation or septic shock requiring vasoconstrictor therapy.

Secondary standards:(only if 3 items are met) Disturbance of consciousness; respiratory rate ≥ 30 times/min; PaO2/FiO2 ≤ 250, or PaO2 \< 60mmHg; azotemia (BUN ≥ 7.12mmol / L); hypotension requires strong fluid resuscitation; infiltration of multiple lobes; leucopenia (WBC \< 4 × 109 / L); thrombocytopenia (\< 10 × 109 / L); hypothermia (T \< 36 ℃).

Exclusion Criteria

* refuse to sign informed consent; inaccurate results due to unqualified sputum or BALF samples
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chaoyang Central Hospital

OTHER

Sponsor Role collaborator

Yingkou Central Hospital

UNKNOWN

Sponsor Role collaborator

Huludao central hospital

UNKNOWN

Sponsor Role collaborator

Dandong First Hospital

UNKNOWN

Sponsor Role collaborator

Fushun Mining Bureau General Hospital

UNKNOWN

Sponsor Role collaborator

Benxi Cental Hospital

OTHER

Sponsor Role collaborator

Shengjing Hospital

OTHER

Sponsor Role lead

Responsible Party

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Hongyu Zhao

deputy director of emergency department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Shengjing hospital of China Medical University

Shenyang, Liaoning, China

Site Status

Countries

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China

Other Identifiers

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PMASP

Identifier Type: -

Identifier Source: org_study_id

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