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Anticoagulant Therapy and 28-days Mortality in Critically Ill COVID-19 Patients

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Karolinska Institute

Status

Completed

Conditions

Thromboembolic Events
Covid-19
Bleeding

Treatments

Drug: Dose of Tinzaparin or Dalteparin

Study type

Observational

Funder types

Other

Identifiers

NCT04412304
Anticoagulant therapy Covid-19

Details and patient eligibility

About

The aims of the study are to to associate anticoagulation (AC) regime with outcome in critically ill patients with Covid-19. This will be done by describe baseline characteristics and comorbidities before hospital admission, level of organ support and dose of AC treatment and associate this with 28 days survival, survival outside ICU, thromboembolic event and bleeding complications.

Enrollment

166 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • laboratory confirmed positive test for SARS-CoV-2
  • admitted to ICU because of critical illness due to covid-19

Exclusion criteria

  • patients with treatment for thromboembolic complications at arrival to the ICU
  • short ICU length of stay defined as discharged the same or the following day as ICU admission

Trial design

166 participants in 3 patient groups

thrombose prophylaxis
Description:
The dose used to prevent thromboembolic complication in critically ill
Treatment:
Drug: Dose of Tinzaparin or Dalteparin
double thrombose prophylaxis
Description:
Double the dose used to prevent thromboembolic complication in critically ill
Treatment:
Drug: Dose of Tinzaparin or Dalteparin
full dose anticoagulant
Description:
Dose used to treat thromboembolic event
Treatment:
Drug: Dose of Tinzaparin or Dalteparin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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