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临床试验/ISRCTN15645679
ISRCTN15645679终止未知

STOPping Anticoagulation for isolated or incidental subsegmental Pulmonary Embolism

niversity of Birmingham0 个研究点目标入组 1,466 人开始时间: 2020年10月23日最近更新:
适应症

试验速览

阶段
未知
状态
终止
入组人数
1,466

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

性别
All

入选标准

  • 1. Age =18 years
  • 2. SSPE diagnosed by the radiologist at the trial site by CTPA or CT thorax with IV contrast
  • 3. No evidence of proximal deep vein thrombosis on doppler ultrasonography or CT/MR venography
  • 4. Heart rate <110 bpm
  • 5. Systolic blood pressure =100 mmHg
  • 6. Oxygen saturation =90%
  • 7. Written signed informed consent to the trial

排除标准

  • 1. Indication for hospital admission
  • 2. >7 days empirical anticoagulation treatment immediately prior to randomisation
  • 3. <28 days since first symptoms of proven or clinically suspected COVID-19
  • 4. Known stage 5 chronic kidney disease
  • 5. Patients with active cancer defined as cancer diagnosed within the past 6 months, cancer for which anticancer treatment was being given at the time of enrolment or during 6 months before randomisation, or recurrent locally advanced or metastatic cancer
  • 6. Patients with previous unprovoked PE, thrombophilia or requiring long term anticoagulation for another reason
  • 7. Patients with a DVT / thrombus of an unusual site (e.g. upper limbs, associated with a line) that requires anticoagulation
  • 8. Patients with active bleeding
  • 9. Any condition which, in the opinion of the investigator, makes the participant unsuitable for trial entry due to prognosis/terminal illness with a projected survival of less than 3 months
  • 10. Pregnancy confirmed by positive pregnancy test or post-partum period or actively trying to conceive
  • 11. Inability to comply with the trial schedule and follow-up
  • 12. Participation in a CTIMP study

研究者

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