Immune response in critically ill patients suffering from pneumonia

Recruiting

• Conditions: pneumoniasepsis

• Registration Number: DRKS00027833
• Lead Sponsor: Klinik für AnästhesiologieUniversitätsmedizin Göttingen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-01-20
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Inpatient treatment in one of the participating intensive care units
- Presence of a diagnosis of pneumonia on admission or during the course of treatment
- Community acquired pneumonia (CAP)
- Hospital acquired pneumonia (HAP)
- Ventilator acquired pneumonia (VAP)
- Signed declaration of consent by the patient or alternatively by the legal representative in case of full legal capacity
- Completion of the 18th year of life

Exclusion Criteria

The following criteria lead to the exclusion or not possible inclusion of patients:
- Lack of informed consent
- Missing pneumonia diagnosis
- Patient included in an intervention study
- Contraindication for further blood collection (acute bleeding etc.)
- Absence of an inserted catheter suitable for collection
- Patient age under 18 years

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Secondary Infection Sepsis (Diagnosis made by intensive care physician)

Secondary Outcome Measures

Name	Time	Method
Inflammatory markers