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Comparison · NCT03045406-deaths

Apixaban vs Dalteparin: deaths from any cause

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. Apixaban vs Dalteparin: deaths from any cause. Trial comparisons, record NCT03045406-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03045406-deaths

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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 10.2340.2020.271wilson
Risk in group 20.2640.230.302wilson
Risk difference, group 1 minus group 2-0.0299-0.07960.02newcombe hybrid score
Risk ratio, group 1 over group 20.8870.7261.08log
Odds ratio, group 1 over group 20.8520.6531.11log
Number needed to treat, for one fewer death from any cause on Apixaban than on Dalteparin33.5from 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 1Apixabanorally administered, at the dose of 10 mg bid for 7 days, followed by 5 mg bid (total period of treatment: six months)~Apixaban: Tablets135576EG000
Group 2Dalteparinsubcutaneously administered, at a dose of 200 IU/kg SC o.i.d for 1 month. Thereafter, dalteparin will be administered at a dose of 150 IU/kg o.i.d. for 5 months~Dalteparin: Injections153579EG001

Harm

What it counts
Total, all-cause mortality
Time frame
6 months treatment + 1 month follow-up

Source ClinicalTrials.gov

Trial

Title
Apixaban for the Treatment of Venous Thromboembolism in Patients With Cancer
NCT number
NCT03045406
Phases
PHASE3
Conditions
Venous Thromboembolism
Interventions
Apixaban, Dalteparin
Lead sponsor
Fadoi Foundation, Italy
Results first posted
2025-06-18

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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