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NCT07664358
Fibrinogen-to-Albumin Ratio as a Predictor of Acute Respiratory Distress Syndrome in Traumatic Brain Injury
Conditions: Fibrinogen, Albumin, ARDS, TBI (Traumatic Brain Injury)
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 350
Sponsor: Tanta University
Location: Tanta University Hospitals Tanta Gharbia Governorate
Summary
this study aims to assess the ability of fibrinogen-to-albumin ratio to predict the development of Acute respiratory distress syndrome in traumatic brain injury patients.
Eligibility Criteria
Inclusion Criteria:
* Patients ≥ 18 years admitted to the ICU with traumatic Brain Injury
* Admission to the ICU within 24 hours of injury.
* Patients will be expected to remain under hospital care for follow-up
* Availability of fibrinogen and albumin measurements within the first 24 hours of ICU admission.
* Informed consent will be obtained from a legally authorized representative.
Exclusion Criteria:
* Preexisting advanced chronic liver disease, nephrotic syndrome, or protein-losing enteropathy.
* Pre-existing ARDS on admission.
* Recipient of albumin, fibrinogen concentrate, or cryoprecipitate before admission sampling.
* Use of anticoagulant or fibrinolytic therapy before admission.
* Active malignancy or severe systemic infection at admission.
* Direct sever lung injury
* Pregnancy
* Refusal of consent
Source: ClinicalTrials.gov (NCT07664358). StuddyBuddy aggregates publicly available trial information.