Mechanisms for Organ Dysfunction in Covid-19

  • STATUS
    Recruiting
  • End date
    Dec 31, 2021
  • participants needed
    300
  • sponsor
    Uppsala University
Updated on 16 April 2021
covid-19

Summary

The study aims to investigate organ dysfunction and biomarkers in patients with suspected or verified COVID-19 during intensive care at Uppsala University Hospital.

Description

Consenting patients with suspected or verified SARS-COV-2 infection, COVID-19, will undergo daily blood, urine and sputum sampling during their stay in intensive care. Data on organ dysfunction will be collected through the electronic patient journal and electronic patient data management system. The collected samples will be analysed for a panel of potential biomarkers that will be correlated to organ dysfunction and clinical outcome.

Details
Condition Pulmonary Disease, Renal Failure, Acute renal failure, Multiple Organ Failure, Toxic Shock Syndrome, ADULT RESPIRATORY DISTRESS SYNDROME, Systemic Inflammatory Response Syndrome, Acute Respiratory Distress Syndrome (ARDS), Kidney Failure (Pediatric), Acute Respiratory Distress, Lung Disease, Kidney Failure, Organ Dysfunction Syndrome Sepsis, *COVID-19, Covid-19, COVID-19, septic shock, SIRS, systemic inflammatory response syndrome (sirs), acute kidney injury, acute respiratory distress syndrome, ards, acute kidney injuries
Clinical Study IdentifierNCT04316884
SponsorUppsala University
Last Modified on16 April 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Admitted to intensive care
suspected or verified COVID-19

Exclusion Criteria

Pregnancy or breastfeeding
Under-age
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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