跳至主要内容
临床试验/PER-056-04
PER-056-04已完成未知

MULTINATIONAL CLINICAL TRIAL, MULTICENTRIC, PHASE II PROSPECTIVE, RANDOMIZED, PARTIALLY BLIND, OF PARALLEL GROUPS, CONTROLLED WITH AN UNDASMATED ACTIVE COMPARATOR OF DOSE SEARCH AND EVALUATION OF DRUG BAY 59-7939 (DIRECT ORAL INHIBITOR OF FACTOR XA) IN THE TREATMENT OF PATIENTS WITH TRUNBOSIS VENOUS DEEP PROXIMAL ACUTE SYMPTOMATIC (STUDIO ODIXA-DVT)

BAYER S.A.,0 个研究点目标入组 0 人开始时间: 2004年9月23日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients with acute symptomatic proximal deep vein thrombosis.
  • Men or women over 18 years of age.

排除标准

  • Contraindication to comparator drugs
  • Symptomatic Pulmonary embolism
  • Conditions with increased bleeding risk
  • Unstable patients with reduced life expectancy
  • Severe renal impairment
  • Impaired liver function
  • Strong CYP 3A4 inhibitors
  • Platelet aggregation inhibitors (exception: ASA up to 500mg) therapy with anticoagulants or fibrinolytics
  • NSAIDs with half-life > 17 hours

研究者

发起方
BAYER S.A.,

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