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Comparison · NCT03477006-0445ffa1

LTLR-WB vs Standard Care: Incidence of Multiple Organ Failure

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. LTLR-WB vs Standard Care: Incidence of Multiple Organ Failure. Trial comparisons, record NCT03477006-0445ffa1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03477006-0445ffa1

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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 20.1960.1070.332wilson
Risk difference, group 1 minus group 2-0.0957-0.2450.0624newcombe hybrid score
Risk ratio, group 1 over group 20.5110.171.53log
Odds ratio, group 1 over group 20.4570.1291.62log
Number needed to treat, for one fewer participant with the outcome on LTLR-WB than on Standard Care10.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: standard care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1LTLR-WB
Receiving 2 units of low titer, leucocyte reduced, platelet replete whole blood initiated in the prehospital setting during air medical transport and continued (up to 6 units of whole blood followed by standard component resuscitation) thru the early in-hospital phase of care~Whole blood: Low titer, group O, leukocyte reduced, platelet replete, cold stored whole blood
440OG000
Group 2Standard CareReceiving standard prehospital air medical care and standard of care component (1:1:1) trauma resuscitation thru the early in-hospital phase of care946OG001

Outcome

Type
SECONDARY
Title
Incidence of Multiple Organ Failure
Description
multiple organ failure using the Denver post-injury MOF score which is a summed score and when the score is 4 or greater from 4 organ system scores, MOF is designated; 4 organ systems (pulmonary \[0-3\], renal \[0-3\], hepatic \[0-3\], cardiovascular \[0-3\])
Time frame
28 days from admission
Population

Source ClinicalTrials.gov

Trial

Title
Pragmatic Prehospital Group O Whole Blood Early Resuscitation Trial
NCT number
NCT03477006
Phases
PHASE3
Conditions
Hemorrhagic Shock
Interventions
Whole blood
Lead sponsor
Jason Sperry
Results first posted
2021-10-06

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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