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Trial · NCT01139658

Results by group54

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Occurrence of Symptomatic Venous Thromboembolic EventsTotal Knee Replacement19participants
Occurrence of Symptomatic Venous Thromboembolic EventsTotal Hip Replacement5participants
Occurrence of Major Bleeding EventsTotal Knee Replacement8participants
Occurrence of Major Bleeding EventsTotal Hip Replacement16participants
Dosage of Pradaxa at InitiationTotal Knee Replacement75 mg/day142participants
Dosage of Pradaxa at InitiationTotal Hip Replacement75 mg/day162participants
Dosage of Pradaxa at InitiationTotal Knee Replacement110 mg/day394participants
Dosage of Pradaxa at InitiationTotal Hip Replacement110 mg/day417participants
Dosage of Pradaxa at InitiationTotal Knee Replacement150 mg/day80participants
Dosage of Pradaxa at InitiationTotal Hip Replacement150 mg/day122participants
Dosage of Pradaxa at InitiationTotal Knee Replacement220mg/day130participants
Dosage of Pradaxa at InitiationTotal Hip Replacement220mg/day228participants
Duration Between Surgery and First Dose of PradaxaTotal Knee Replacement12.6Standard Deviation 14.5hours
Duration Between Surgery and First Dose of PradaxaTotal Hip Replacement14.6Standard Deviation 16.8hours
Duration of TreatmentTotal Knee Replacement27.5Standard Deviation 11.8days
Duration of TreatmentTotal Hip Replacement33.3Standard Deviation 10.4days
Proportion of Patients With a Preoperative ALT MeasurementTotal Knee Replacement73.3percentage of participants
Proportion of Patients With a Preoperative ALT MeasurementTotal Hip Replacement74.5percentage of participants
Adherence to TreatmentTotal Knee Replacement98.6Standard Deviation 24.6percent
Adherence to TreatmentTotal Hip Replacement97.3Standard Deviation 24.6percent

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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