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NCT05374018 Clinical Trial

Urinary Antigen Test for Stretococcus Pneumoniae Serotype Prevalence in Community Acquired Pneumonia

Pneumonia Clinical Trial

Official title:
Prospective Study to Evaluate Stretococcus Pneumoniae Serotype Prevalence in Community Acquired Pneumonia in Hong Kong Using a Urinary Kit

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05374018
Other study ID # CREC 2020.34
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2021
Est. completion date December 31, 2024

Study information
Verified date February 2024
Source Chinese University of Hong Kong
Contact KW To, MBChB
Phone 35052211
Email tokw617@yahoo.com.hk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is an epidemiology study for the prevalence and serotypes of pneumococcus pneumoniae in hospitalized patients with community acquired pneumonia (CAP). The serotypes of the pneumococcus pneumoniae will be determined by a urinary antigen assay

Recruitment information / eligibility
Status Recruiting
Enrollment 1800
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Admitted with signs and symptoms suggestive of pneumonia which include one or more of the followings: 1. fever 2. CXR changes with consolidation, increased alveolar shadowing or hazziness 3. respiratory symptoms like increase shortness of breath, cough with sputum Raised inflammatory markers suggesting of bacterial infection with either increased white cell count or C-reactive protein, or both Exclusion Criteria: - Nosocomial pneumonia which is acquired >= 48 hours after hospital admission. Pneumonia which are already known to be caused by pathogens other than pneumococcus pneumoniae.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• urinary kit for pneumococcus antigen assay
urine test for detection of pneumococcus antigen

Locations
Country Name City State
Hong Kong Department of Medicine and Therapeutics, Prince of Wales Hospital, CUHK Shatin

Sponsors (1)
Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome
Type Measure Description Time frame Safety issue
Primary prevalence of strep pneumonia to determine prevalence 2 years
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