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Comparison · NCT02285153-b3f949c8

Acetylsalicylic Acid Lysinate vs 0.9% Sodium-chloride Solution: Intensive Care Unit 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. Acetylsalicylic Acid Lysinate vs 0.9% Sodium-chloride Solution: Intensive Care Unit Mortality. Trial comparisons, record NCT02285153-b3f949c8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02285153-b3f949c8

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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 10.2860.08220.641wilson
Risk in group 20.1250.02240.471wilson
Risk difference, group 1 minus group 20.161-0.2410.531newcombe hybrid score
Risk ratio, group 1 over group 22.290.2620.1log
Odds ratio, group 1 over group 22.80.19640.1log
Number needed to treat, for one more participant with the outcome on Acetylsalicylic Acid Lysinate than on 0.9% Sodium-chloride Solution6.22from 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 1Acetylsalicylic Acid Lysinate100mg Acetylsalicylic Acid~Acetylsalicylic acid lysinate: 100mg intravenously administered Acetylsalicylic Acid lysinate per day27OG000
Group 20.9% Sodium-chloride Solution0.9% sodium-chloride solution~0.9% sodium-chloride solution: Placebo, intravenously administered, daily18OG001

Outcome

Type
SECONDARY
Title
Intensive Care Unit Mortality
Description
Mortality of patients during their intensive care unit stay, 90 day mortality, potentially longer
Time frame
up to 90 days after inclusion
Population

Source ClinicalTrials.gov

Trial

Title
Does Acetylsalicylic Acid Reduce the Mortality of Patients Admitted to an Intensive Care Unit
NCT number
NCT02285153
Phases
PHASE3
Conditions
Critical Illness
Interventions
Acetylsalicylic acid lysinate, 0.9% sodium-chloride solution
Lead sponsor
Medical University of Vienna
Results first posted
2019-12-18

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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