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Prevention of Venous Thromboembolic Events After Elective Orthopaedic Surgery in Patients Treated With PRADAXA

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Venous Thromboembolism

Study type

Observational

Funder types

Industry

Identifiers

NCT01139658
1160.102

Details and patient eligibility

About

Observational cohort study on the prevention of venous thromboembolic events after elective orthopaedic surgery for Total Knee Replacement or Total Hip Replacement iin patients treated with PRADAXA to evaluate the efficacy ant safety of Pradaxa in real-life conditions

Enrollment

1,676 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients treated with Pradaxa undergoing surgery for Total Knee Replacement or Total Hip Replacement
  2. Patients 18 years of age or older at the time of recruitment

Exclusion criteria

  1. Patients presenting contraindication to prescription of Pradaxa
  2. Patients in whom long term Anti vitamin K treatment is indicated

Trial design

1,676 participants in 1 patient group

All comers

Trial contacts and locations

53

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Data sourced from clinicaltrials.gov

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