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Trial · NCT03784794

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of Blood products transfused24 hrsNumber of allogeneic blood products transfused intra-op, within 24h after screening and in-hospital (RBC, Platelets and FFP; separate and overall)
SecondaryNumber of hemocomponents or fibrinogen concentrates needed to treat hypofibrinogenemiaday 0 to day 15Number of packs of Cryo (pack of 5 \~ 1 G Fibrinogen), Fibrinogen Concentrate (G), and PCC (500 UI) administered intra-operating
SecondaryIncidence of Red Blood Cells transfusion (RBC)day 0 to day 15Incidence ≥ 5 U RBC transfused
SecondaryIncidence of Massive Red Blood Cells transfusion (RBC)day 0 to day 15Incidence ≥ 10 U RBC transfused (first 24h after screening)
Secondaryestimated blood lossday 0 to day 15Overall estimated blood loss (EBL, ML)
SecondaryTime to bleeding control24 hrstime from study entry to last hemostatic intervention/transfusion
SecondaryIncidence of coagulopathyday 0 to day 15detected by thromboelastometry or standard coagulation laboratory tests
SecondaryIncidence of hysterectomyday 0 to day 15number of obstetric hysterectomy for bleeding control
SecondaryIncidence of re-surgeryday 0 to day 15number of procedures necessary for bleeding control
SecondaryIncidence of Transfused associated circulatory overloadday 0 to day 15number of patients with transfused associated circulatory overload
SecondaryIncidence of surgical site infection or sepsisday 0 to day 15number of patients that developed health care related infections or sepsis
SecondaryIncidence of ICU admissionday 0 to day 15number of patients that require admission to the ICU for complications related to hipovolemic shock
SecondaryIn-hospital mortalityday 0 to day 15number of deaths

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT03784794/registered