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Completed

NCT Number: NCT00329628

Rivaroxaban (10mg) Given Once Daily in Patients Undergoing Total Hip Replacement Compared to Enoxaparin

The purpose of this study is to assess if 10 mg BAY 59-7939, taken once daily as a tablet, is safe and prevent blood clot which may form after total hip replacement operation.

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Key information

Conditions

Venous Thromboembolism Cardiovascular Diseases Embolism and Thrombosis Thromboembolism Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Avellaneda, Buenos Aires, Argentina

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female patients aged 18 years or above
  • Patients scheduled for elective total hip replacement

Exclusion criteria

  • Planned, staged total bilateral hip replacement
  • Active bleeding or high risk of bleeding contraindicating treatment with low molecular weight heparin
  • Contraindication listed in the labeling or conditions precluding patient treatment with enoxaparin
  • Conditions prohibiting bilateral venography (e.g. amputation of one leg, allergy to contrast media)

Treatment and study plan

Rivaroxaban (BAY59-7939)

Drug

10 mg OD tablet of rivaroxaban administered for 36 +/- 4 days

Enoxaparin

Drug

Syringe of Enoxaparin active substance at a dose of 40 mg administered for 13 +/- 2 days

Primary outcomes

  1. Composite endpoint of total VTE i.e.: Any DVT (proximal and/or distal), Non fatal PE, Death of all causes

    Time frame: Treatment period : up to day 36+/-6

Secondary outcomes

  1. Incidence of the composite endpoint comprising proximal DVT, non-fatal PE and VTE- related death (major VTE)

    Time frame: Treatment period : up to day 36+/-6

  2. Incidence of symptomatic VTE (DVT, PE)

    Time frame: Treatment period : up to day 36+/-6

  3. Incidence of DVT (total, proximal, distal)

    Time frame: Treatment period : up to day 36+/-6

  4. Incidence of symptomatic VTE during follow-up

    Time frame: Follow-up period: following 36+/-6 days

  5. The composite endpoint comprising major VTE and treatment-emergent major bleeding

    Time frame: For major VTE, treatment period: up to Day 36+/-6 ; for major bleeding, from first dose of double-blind study medication to up to two days after last dose of double-blind study medication

  6. Incidence of the composite endpoint that results from the primary endpoint by substituting VTE related death for all death

    Time frame: Treatment period : up to day 36+/-6

  7. Incidence of the composite endpoint that results from major VTE by substituting all cause mortality for VTE-related death

    Time frame: Treatment period : up to day 36+/-6

  8. Treatment-emergent major bleedings

    Time frame: From first dose of double-blind study medication to up to two days after last dose of double-blind study medication

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

RECORD 1 Study: REgulation of Coagulation in ORthopedic Surgery to Prevent DVT and PE, Controlled, Double-blind, Randomized Study of BAY 59-7939 in the Extended Prevention of VTE in Patients Undergoing Elective Total Hip Replacement

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
May 25, 2006
Registry last updated
Oct 28, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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