PLAIAR-Trial: Platelets in Inflammation and Resolution
- Conditions
- ARDSPlatelet Abnormality
- Registration Number
- NCT05098106
- Lead Sponsor
- University Hospital Muenster
- Brief Summary
Detection and determination of platelets in bronchoalveolar lavage fluid and blood in ARDS and non-ARDS-patients. Correlation with phenotype and inflammation parameters in blood and outcome parameters.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 72
Inclusion Criteria
- Routine bronchoscopy
- Patient in perioperative setting
- Age >=18 years
- Consent
Exclusion Criteria
- Active or recent (in past 7 days) bleeding in upper airways
- Recent traumatic injury of the lung associated with (micro-)hemorrhage
- Blood aspiration
- Pregnancy
- Age<18 years
- Acute kidney injury / Chronic kidney failure / Dialysis
- Transplantation
- HIV
- Hematologic diseases
- Immunosuppression
- Anti-Platelet-Therapy
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detectability and changes in platelets in BAL and blood 5-7 days Organ failure, survival. 1 Year Systemic platelet and leukocyte numbers 5-7 days Systemic platelet and leukocyte phenotypes. 5-7 days Systemic cytokine profiles. 5-7 days
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms link platelet activation to inflammation resolution in ARDS patients as studied in NCT05098106?
How does bronchoalveolar lavage platelet analysis compare to standard-of-care biomarkers in predicting ARDS outcomes?
Which platelet-derived biomarkers correlate with ARDS severity and resolution in blood and BALF samples from NCT05098106?
What are the potential adverse events of bronchoscopy in ARDS patients and how do they impact platelet function assessment?
How do platelet function inhibitors or activators interact with ARDS pathophysiology based on findings from NCT05098106?
Trial Locations
- Locations (1)
University Hospital Muenster
🇩🇪Muenster, Germany
University Hospital Muenster🇩🇪Muenster, GermanyCarola Wempe, Dr.Contact+4925147255wempe-c@anit.uni-muenster.deAndreas Margraf, Dr.Contactandreas.margraf@anit.uni-muenster.de