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Comparison · NCT00657150-4a496049

Dabigatran 220mg vs Enoxaparin: Number of Participants With Total Venous Thromboembolic Event and All-cause Mortality During Treatment Period

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. Dabigatran 220mg vs Enoxaparin: Number of Participants With Total Venous Thromboembolic Event and All-cause Mortality During Treatment Period. Trial comparisons, record NCT00657150-4a496049. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00657150-4a496049

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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 10.0770.06040.0977wilson
Risk in group 20.08780.070.11wilson
Risk difference, group 1 minus group 2-0.0108-0.03820.0165newcombe hybrid score
Risk ratio, group 1 over group 20.8770.6311.22log
Odds ratio, group 1 over group 20.8670.6051.24log
Number needed to treat, for one fewer participant with the outcome on Dabigatran 220mg than on Enoxaparin92.9from 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 1Dabigatran 220mgqd (once daily) oral61792OG000
Group 2Enoxaparin40mg qd (once daily) subcutaneous69786OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Total Venous Thromboembolic Event and All-cause Mortality During Treatment Period
Description
Total Venous Thromboembolic Event (VTE) includes both proximal and distal deep vein thrombosis (DVT) (detected by routine venography), symptomatic DVT (confirmed by venous duplex, ultrasound, venography or autopsy) and pulmonary embolism (PE) (confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy).~All of these components and all deaths were centrally adjudicated by the VTE events committee, which was not aware of the treatment allocation of the patients.
Time frame
28-35 days
Population
Full Analysis Set (randomised, had taken at least 1 dose of oral or subcutaneous trial medication, had undergone surgery, had evaluable negative venogram for both distal and proximal DVT in both legs or positive venography in any 1 segment of 1 or both legs, or confirmed symptomatic DVT, PE or death during the treatment period.)

Source ClinicalTrials.gov

Trial

Title
Dabigatran Etexilate Compared With Enoxaparin in Prevention of Venous Thromboembolism (VTE) Following Total Hip Arthroplasty
NCT number
NCT00657150
Phases
PHASE3
Conditions
Venous Thromboembolism
Interventions
Enoxaparin, Dabigatran etexilate
Lead sponsor
Boehringer Ingelheim
Results first posted
2010-12-17

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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