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PLAIAR-Trial: Platelets in Inflammation and Resolution

Conditions
ARDS
Platelet 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
NameTimeMethod
Detectability and changes in platelets in BAL and blood5-7 days
Organ failure, survival.1 Year
Systemic platelet and leukocyte numbers5-7 days
Systemic platelet and leukocyte phenotypes.5-7 days
Systemic cytokine profiles.5-7 days
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital Muenster

🇩🇪

Muenster, Germany

University Hospital Muenster
🇩🇪Muenster, Germany
Carola Wempe, Dr.
Contact
+4925147255
wempe-c@anit.uni-muenster.de
Andreas Margraf, Dr.
Contact
andreas.margraf@anit.uni-muenster.de

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