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Clinical Trials/EUCTR2011-000766-35-ES
EUCTR2011-000766-35-ESActive, not recruitingNot Applicable

Prevención del sangrado postoperatorio en artroplastia total de rodilla: Ensayo clínico multicéntrico, aleatorizado, abierto, paralelo de tres brazos de tratamiento, que evalúa la eficacia del ácido tranexámico endovenoso y tópico versus hemostasia habitual

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau0 sitesStarted: September 29, 2011Last updated:
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Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
All

Inclusion Criteria

  • •1.Pacientes mayores de 18 años
  • •2.Intervención de artroplastia total de rodilla
  • •3.Firma del consentimiento informado del paciente
  • •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 50
  • •F.1.3 Elderly (>=65 years) yes
  • •F.1.3.1 Number of subjects for this age range 100

Exclusion Criteria

  • •Alergia conocida al ATX.
  • •Accidente vascular cerebral (AVC, AIT)
  • •Cardiopatía isquémica (IAM, ángor)
  • •Trombosis venosa profunda (TVP) y/o superficial
  • •Tromboembolismo Pulmonar (TEP) Vasculopatía arterial periférica
  • •Tratamiento con hierro en el post-operatorio
  • •Uso de recuperadores de sangre durante la intervención quirúrgica
  • •Pacientes con arritmias trombogénicas (ejempl: AcxFA)
  • •Pacientes portadores de prótesis cardiovasculares
  • •Alteraciones de la coagulación protrombóticas Tratamiento con fármacos anticonceptivo

Investigators

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

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