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Comparison · NCT01139658-56b79376

Total Knee Replacement vs Total Hip Replacement: Number of Patients Who Switched to Another Anticoagulant Therapy

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. Total Knee Replacement vs Total Hip Replacement: Number of Patients Who Switched to Another Anticoagulant Therapy. Trial comparisons, record NCT01139658-56b79376. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01139658-56b79376

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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 10.05760.04310.0767wilson
Risk in group 20.04840.03640.0642wilson
Risk difference, group 1 minus group 20.0092-0.01230.0318newcombe hybrid score
Risk ratio, group 1 over group 21.190.7921.79log
Odds ratio, group 1 over group 21.20.7821.85log
Number needed to treat, for one more participant with the outcome on Total Knee Replacement than on Total Hip Replacement109from 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 1Total Knee ReplacementPatients undergoing elective total knee replacement (TKR) received a dose of dabigatran etexilate; the administered treatment was based on usual practice in a real-life setting.43746OG000
Group 2Total Hip ReplacementPatients undergoing elective total hip replacement (THR) received a dose of dabigatran etexilate; the administered treatment was based on usual practice in a real-life setting.45929OG001

Outcome

Type
SECONDARY
Title
Number of Patients Who Switched to Another Anticoagulant Therapy
Description
Treated population included patients who took at least one dose of Pradaxa. One additional patient was excluded from the analysis as they were missing their date of first dose.
Time frame
11 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Prevention of Venous Thromboembolic Events After Elective Orthopaedic Surgery in Patients Treated With PRADAXA
NCT number
NCT01139658
Phases
Conditions
Venous Thromboembolism
Interventions
Lead sponsor
Boehringer Ingelheim
Results first posted
2014-01-16

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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