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Pradaxa (Dabigatran Etexilate) VTE Prevention After Elective Total Hip or Knee Replacement Surgery

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Terminated

Conditions

Venous Thromboembolism
Arthroplasty, Replacement

Treatments

Drug: dabigatran

Study type

Observational

Funder types

Industry

Identifiers

NCT01153698
1160.118

Details and patient eligibility

About

an open, prospective, observational study to collect data on safety (major bleeding events) and efficacy (symptomatic venous thromboembolism(VTE)) of a switch from Enoxaparin to dabigatran etexilate in patients with total knee replacement (TKR) and total hip replacement (THR)

Enrollment

167 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

patients age 18 years or above undergoing elective total hip or knee replacement surgery

Exclusion criteria

according to the label recommendation for Pradaxa 220 mg QD

Trial design

167 participants in 1 patient group

patients after hip or knee replacement
Treatment:
Drug: dabigatran

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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