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Clinical Trials/EUCTR2009-017804-95-ES
EUCTR2009-017804-95-ES
Active, not recruiting
Not Applicable

Prevención del sangrado postoperatorio: Ensayo clínico unicéntrico, aleatorizado, paralelo y controlado que evalúa la eficacia de la cola de fibrina y el ácido tranexámico en pacientes intervenidos de artroplastia total de rodilla.

Fundació Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau0 sitesDecember 30, 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Fundació Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 30, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Fundació Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau

Eligibility Criteria

Inclusion Criteria

  • Patients older than 18 years
  • Intervention of primary total knee arthroplasty
  • Patient consent to participate in the study
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Hypersensibility to the study drugs or the bovine proteins (aprotinin)
  • History of thromboembolic disease:
  • ?Cerebrovascular accident
  • ?Ischaemic cardiopathy
  • ?Deep thrombosis venous and/or superficial
  • ?Lung thromboembolism
  • ?Periferical arterial vasculopathy
  • Patients with thromboembolic arrhythmias (AcxFA)
  • Patients with cardiovascular prosthesis
  • Coagulations prothrombotic disease

Outcomes

Primary Outcomes

Not specified

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