跳至主要内容
临床试验/NL-OMON54327
NL-OMON54327招募中不适用

eiden Thrombosis Recurrence Risk Prevention: Tailored treatment after a first venous thromboembolism: (L-TRRiP study) - L-TRRiP study

eids Universitair Medisch Centrum0 个研究点目标入组 1,600 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
1,600

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

年龄范围
18 至 99(—)

入选标准

  • 1. Provision of informed consent prior to any study specific procedures.
  • 2. Be diagnosed with a first confirmed symptomatic deep vein thrombosis
  • (including distal vein thrombosis, in Dutch ' kuitvenetrombose') or pulmonary
  • embolism with an indication for treatment with anticoagulant therapy for at
  • least 3 months as prescribed by their treating physician.
  • 3. Be aged 18 years or above.

排除标准

  • 1. Patients with active cancer (i.e. cancer diagnosis within six months before
  • VTE (excluding basal-cell or squamous-cell carcinoma of the skin), recently
  • recurrent or progressive cancer or any cancer that required anti-cancer
  • treatment within six months before the venous thromboembolism was diagnosed) or
  • antiphospholipid syndrome
  • 2. Patients who need to continue anticoagulant treatment for another indication
  • (e.g. atrial fibrillation).
  • 3. Patients with a strong indication for long-term antiplatelet therapy despite
  • oral anticoagulation (e.g. those with recent STEMI)
  • 4. Patients with COVID-19 associated VTE (i.e. hospital admission because of
  • COVID-19 <3 months before VTE) or vaccine-induced immune thrombotic
  • thrombocytopenia (VITT)
  • 5. Patients in whom the risk of bleeding is deemed extremely high by the
  • treating physician, necessitating discontinuation of anticoagulant treatment
  • for the first VTE after the initial 3 months or even during the initial 3

研究者

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