Fibrinogen Early In Severe Trauma studY Junior
關鍵詞
抽象
日期
最後驗證: | 05/31/2020 |
首次提交: | 03/22/2018 |
提交的預估入學人數: | 04/15/2018 |
首次發布: | 04/24/2018 |
上次提交的更新: | 06/24/2020 |
最近更新發布: | 06/28/2020 |
實際學習開始日期: | 06/30/2018 |
預計主要完成日期: | 06/29/2021 |
預計完成日期: | 06/29/2021 |
狀況或疾病
干預/治療
Drug: Fibrinogen Concentrate
Drug: Cryoprecipitate
相
手臂組
臂 | 干預/治療 |
---|---|
Experimental: Fibrinogen Concentrate Fibrinogen Replacement using Fibrinogen Concentrate as per ROTEM (FIBTEM) FIBTEM A5 0mm = 60mg/kg FC FIBTEM A5 1-4mm = 50mg/kg FC FIBTEM A5 5-6mm = 40mg/kg FC FIBTEM A5 7-8mm = 30mg/kg FC FIBTEM A5 9-10mm = 20mg/kg FC | Drug: Fibrinogen Concentrate Experimental |
Active Comparator: Cryoprecipitate Fibrinogen Replacement using Cryoprecipitate as per ROTEM (FIBTEM) FIBTEM A5 0mm = 6ml/kg Cryoprecipitate FIBTEM A5 1-4mm = 5ml/kg Cryoprecipitate FIBTEM A5 5-6mm = 4ml/kg Cryoprecipitate FIBTEM A5 7-8mm = 3ml/kg Cryoprecipitate FIBTEM A5 9-10mm = 2ml/kg Cryoprecipitate | Drug: Cryoprecipitate Comparator |
資格標準
有資格學習的年齡 | 3 Months 至 3 Months |
有資格學習的性別 | All |
接受健康志願者 | 是 |
標準 | Inclusion Criteria: 1. Child affected by trauma (3 months to 18 years) 2. Judged to have significant haemorrhage OR predicted to require significant transfusion by the treating clinician 3. Activation of Local MHP or transfusion of emergency red blood cells (Pre-hospital or at Trauma Centre) Exclusion Criteria: 1. Injury judged incompatible with survival 2. Randomisation unable to occur within 6 hours of hospital admission 3. Pregnancy 4. Known personal or parental objection to blood products 5. Known coagulation disorder (i.e. haemophilia, von Willebrand disease) 6. Previous dedicated fibrinogen replacement this admission 7. Pre-Trauma Centre dedicated fibrinogen replacement 8. Participation in competing study |
結果
主要結果指標
1. Time to administration of fibrinogen replacement from time of identification of hypofibrinogenaemia requiring fibrinogen replacement [3 Hours]
次要成果指標
1. Transfusion Requirements [Up to 48 hours after Trauma Unit presentation]
2. Duration of bleeding episode or time until surgical control [It is anticipated that haemorrhage control will be achieved within 12 hours]
3. Intensive Care Unit LOS [1 Year]
4. Hospital LOS [1 Year]
5. Adverse Events [1 Year]
6. All Cause Mortality [Up to 90 Days]
7. Functional Outcomes GOS-E Paediatrics [Up to 90 Days]