Comparison, optimization en evaluation of new and fast molecular diagnostic techniques for detection of atypical bacterial respiratory tract pathogens in clinical samples from patients with CAP.

Completed

• Conditions: Atypical pneumonia; respiratory tract infection; 10004018; 10024970

• Registration Number: NL-OMON32296
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 300

Inclusion Criteria

All patients with symptoms of CAP.

Exclusion Criteria

Patients will be excluded from the study if they disagree with the conditions as mentioned in the informed consent or if investigator believes that subject is not suitable for inclusion in the study (i.e. not compliant with subject requirements).

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters are the results obtained with the different molecular<br /><br>diagnostic methods.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary study parameter will be the results obtained for the different<br /><br>clinical materials.</p><br>