跳至主要内容
临床试验/CTRI/2021/03/032293
CTRI/2021/03/032293尚未招募3 期

Randomised, Embedded, Multifactorial, Adaptive, Platform Trial for Community-Acquired Pneumonia (REMAP-CAP) â?? Therapeutic anticoagulation in COVID-19 - REMAP-CAP

Monash University0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募

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

  • 1. Adult patient admitted to an ICU for acute severe CAP within 48 hours of hospital admission with
  • a. symptoms or signs or both that are
  • consistent with lower respiratory tract
  • infection (for example, acute onset of
  • dyspnea, cough, pleuritic chest pain) AND
  • b. Radiological evidence of new onset
  • infiltrate of infective origin (in patients
  • with preexisting radiological changes,
  • evidence of new infiltrate)
  • 2. Up to 48 hours after ICU admission, receiving organ support with one or more of:
  • a. Non-invasive or invasive ventilatory
  • b. Receiving infusion of vasopressor or
  • inotropes or both

排除标准

  • 1. Healthcare-associated pneumonia:
  • a. Prior to this illness, is known to have
  • been an inpatient in any healthcare
  • facility within the last 30 days
  • b. Resident of a nursing home or long-term
  • care facility.
  • 2. Death is deemed to be imminent and inevitable during the next 24 hours AND one or more of the patient, substitute decision maker or attending physician are not committed to full active treatment.
  • 3. Previous participation in this REMAP within the last 90 days
  • 4. Clinical or laboratory bleeding risk or both that is sufficient to contraindicate therapeutic anticoagulation, including intention to continue or commence dual anti-platelet therapy
  • 5. Therapeutic anticoagulation is already present due to prior administration of any anticoagulant agent that is known or likely to still be active or a clinical decision has been made to commence therapeutic anticoagulation
  • 6. Enrolment in a trial evaluating anticoagulation for proven or suspected COVID19 infection, where the protocol of that trial requires continuation of the treatment assignment specified in that trial
  • 7. Known or suspected previous adverse reaction to UFH or LMWH including heparin induced thrombocytopenia (HIT).

研究者

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