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Comparison · NCT02073682-fe1bfa96

Edoxaban Group vs Dalteparin Group: Number of Participants With VTE-Related Death

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. Edoxaban Group vs Dalteparin Group: Number of Participants With VTE-Related Death. Trial comparisons, record NCT02073682-fe1bfa96. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02073682-fe1bfa96

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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 10.01150.005280.0248wilson
Risk in group 20.007630.002970.0195wilson
Risk difference, group 1 minus group 20.00386-0.00950.018newcombe hybrid score
Risk ratio, group 1 over group 21.510.4275.3log
Odds ratio, group 1 over group 21.510.4245.39log
Number needed to treat, for one more participant with the outcome on Edoxaban Group than on Dalteparin Group259from 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 1Edoxaban GroupAfter 5 days of low molecular weight heparin (LMWH), participants received edoxaban treatment daily6522OG000
Group 2Dalteparin GroupParticipants received dalteparin daily4524OG001

Outcome

Type
SECONDARY
Title
Number of Participants With VTE-Related Death
Description
Time frame
12 months
Population
mITT (Safety Analysis Set)

Source ClinicalTrials.gov

Trial

Title
Cancer Venous Thromboembolism (VTE)
NCT number
NCT02073682
Phases
PHASE3
Conditions
Venous Thromboembolism (VTE), Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE), Cancer
Interventions
Edoxaban, Dalteparin, Low molecular weight heparin
Lead sponsor
Daiichi Sankyo
Results first posted
2018-10-24

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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