[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644267":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":24,"locations":31,"responsibleParty":47,"collaborators":10,"id":51,"slug":52,"hasResults":53,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":53,"sex":59,"minAge":60,"maxAge":10,"enrollmentInfo":61,"targetDuration":10,"studyType":64,"phases":10,"briefSummary":65,"conditions":66,"keywords":10,"overallStatus":70,"whyStopped":10,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Tanta University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Acute respiratory distress syndrome group",null,"patients who will develop ARDS within 7 days of ICU admission, defined according to the Berlin criteria. Fibrinogen (g\u002FL) and albumin (g\u002FL) levels in the blood will be measured from the first routine blood sample after ICU admission.\n\nFibrinogen-to-albumin ratio will be calculated as:\n\nFAR = Fibrinogen (g\u002FL)\u002FAlbumin (g\u002FL)",[13],"Diagnostic Test: Fibrinogen-to-albumin ratio",{"label":15,"type":10,"description":16,"interventionNames":17},"Non acute respiratory distress syndrome group","patients who will not develop ARDS within 7 days of ICU admission. Fibrinogen (g\u002FL) and albumin (g\u002FL) levels in the blood will be measured from the first routine blood sample after ICU admission.\n\nFibrinogen-to-albumin ratio will be calculated as:\n\nFAR = Fibrinogen (g\u002FL)\u002FAlbumin (g\u002FL)",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"DIAGNOSTIC_TEST","Fibrinogen-to-albumin ratio","Fibrinogen (g\u002FL) and albumin (g\u002FL) levels in the blood will be measured from the first routine blood sample after ICU admission.\n\nFibrinogen-to-albumin ratio will be calculated as:\n\nFAR = Fibrinogen (g\u002FL)\u002FAlbumin (g\u002FL)",[9,15],[25],{"name":26,"role":27,"phone":28,"phoneExt":29,"email":30},"Eman M Taher, MD","CONTACT","01090822808","002","emantaher6669@gmail.com",[32],{"facility":33,"status":10,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Tanta University Hospitals","Tanta","Gharbia Governorate","31527","Egypt","EG",{"type":40,"coordinates":41},"Point",[42,43],31.00192,30.78847,{"lat":43,"lon":42},[46],{"name":26,"role":27,"phone":28,"phoneExt":29,"email":30},{"type":48,"investigatorFullName":49,"investigatorTitle":50,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Eman Mohammed Taher Salem Abo-Omar","lecturer of anesthesiology, surgical intensive care and pain medicine Tanta university","100644267","fibrinogen-to-albumin-ratio-as-a-predictor-of-acute-respiratory-distress-syndrome-in-traumatic-brain-injury-100644267",false,"NCT07664358","Fibrinogen-to-Albumin Ratio as a Predictor of Acute Respiratory Distress Syndrome in Traumatic Brain Injury","Fibrinogen-to-Albumin Ratio as a Predictor of Acute Respiratory Distress Syndrome in Patients With Traumatic Brain Injury: The Prospective, Observational, Multi-center FARDS Study","FARDS","Inclusion Criteria:\n\n* Patients ≥ 18 years admitted to the ICU with traumatic Brain Injury\n* Admission to the ICU within 24 hours of injury.\n* Patients will be expected to remain under hospital care for follow-up\n* Availability of fibrinogen and albumin measurements within the first 24 hours of ICU admission.\n* Informed consent will be obtained from a legally authorized representative.\n\nExclusion Criteria:\n\n* Preexisting advanced chronic liver disease, nephrotic syndrome, or protein-losing enteropathy.\n* Pre-existing ARDS on admission.\n* Recipient of albumin, fibrinogen concentrate, or cryoprecipitate before admission sampling.\n* Use of anticoagulant or fibrinolytic therapy before admission.\n* Active malignancy or severe systemic infection at admission.\n* Direct sever lung injury\n* Pregnancy\n* Refusal of consent","ALL","18 Years",{"count":62,"type":63},350,"ESTIMATED","OBSERVATIONAL","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.",[67,68,69],"Fibrinogen Albumin Ratio","ARDS","TBI (Traumatic Brain Injury)","NOT_YET_RECRUITING","2026-06-17",{"date":73,"type":74},"2026-06-24","ACTUAL",{"date":76,"type":63},"2026-07-01",{"date":78,"type":63},"2026-12-30",{"name":5,"class":6},1]