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Comparison · NCT05081063-bde393f0

Low Titer O+ Whole Blood vs Component Therapy: Mortality

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Low Titer O+ Whole Blood vs Component Therapy: Mortality. Trial comparisons, record NCT05081063-bde393f0. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05081063-bde393f0

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.10.03960.231wilson
Risk in group 20.1060.06280.172wilson
Risk difference, group 1 minus group 2-0.00569-0.09570.132newcombe hybrid score
Risk ratio, group 1 over group 20.9460.3272.74log
Odds ratio, group 1 over group 20.940.2883.07log
Number needed to treat, for one fewer participant with the outcome on Low Titer O+ Whole Blood than on Component Therapy176from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Low Titer O+ Whole BloodLow Titer O+ Whole blood provided to Level A trauma patients440OG000
Group 2Component TherapyComponent Therapy of O+ pRBC and FFP dispatched to trauma bay for level A traumas13123OG001

Outcome

Type
SECONDARY
Title
Mortality
Description
Assessment of mortality~This is a composite measurement which includes the following in order to be assessed as pulseless with no respiratory drive or brain death:~1. there is no evidence of arousal or awareness to maximal external stimuli~2. pupils are fixed in a midsized or dilated position and non reactive to light~3. corneal, oculocephalic and oculovestibular reflexes are absent~4. There is no facial movement to noxious stimuli~5. the gag reflex is absent to bilateral posterior pharyngeal stimuli~6. the cough reflex is absent to deep tracheal suctioning~7. there is no brain mediated motor response to noxious stimuli of the limbs~8. spontaneous respirations are not observed when apnea test targets reach pH \<7.30 and PaCO2 \>60mmhg
Time frame
In patients surviving at least 24 hours who were included in analysis of outcome measures, we assessed survival to hospital discharge. This means the duration of time in the hospital up to discharge with a maximum of 30 days.
Population

Source ClinicalTrials.gov

Trial

Title
Low-Titer O Positive Whole Blood Versus Component Therapy for Emergent Transfusion in Trauma Patients
NCT number
NCT05081063
Phases
PHASE3
Conditions
Hemorrhagic Shock, Acute Blood Loss Anemia, Traumatic Brain Injury
Interventions
Routine labs
Lead sponsor
Loma Linda University
Results first posted
2025-08-08

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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