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Establishing a COVID-19 Prospective Cohort for Identification of Secondary HLH (COVIDHLH)

T

Technical University of Munich

Status

Unknown

Conditions

COVID

Study type

Observational

Funder types

Other

Identifiers

NCT04347460
161/20 S

Details and patient eligibility

About

SARS-CoV2 has become a pandemic disease putting an enormous burden on health care systems around the world. A considerable amount of patients require intensive care treatment for Covid-19 associated pneumonia. At this point there is no specific treatment, apart from supportive intensive care treatment protocols for severe COVID-19 disease.The latest reports describe massive hyperinflammation in some of the severe COVID-19 patients, which is not a typical finding in virus associated pneumonia. The H-score and the modified HLH 2004 score offer diagnostic tools, that help establishing the diagnosis of HLH. Even more important is the expert clinical judgment to establish the diagnosis of sHLH.

Full description

SARS-CoV2 has become a pandemic disease putting an enormous burden on health care systems around the world. The course of disease is relatively mild in most of the patients, but there is a considerable amount of patients that require intensive care treatment for Covid-19 associated pneumonia. At this point there is no specific treatment, apart from supportive intensive care treatment protocols for severe COVID-19 disease.The latest reports describe massive hyperinflammation in some of the severe COVID-19 patients. The H-score and the modified HLH 2004 score offer diagnostic tools, that helps establishing the diagnosis of HLH. Moreover expert clinical judgment is key to establish a diagnosis of sHLH. Still, so far no systematic analysis has been carried out answering the question as to whether or not these patients suffer from secondary HLH and could potentially benefit from immunomodulatory drugs.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 17a
  • diagnosis of SARS CoV 2 by PCR testing
  • Hospitalized due to clinical severity of the disease
  • written and informed consent or consent of the family
  • GFR<30 is not an exclusion criterion

Exclusion criteria

  • not fulfilling the inclusion criteria
  • missing written and informed consent

Trial design

20 participants in 1 patient group

COVID 19
Description:
Patients requiring ICU treatment due to severe COVID 19 interstitial pneumonia or otherwise COVID-19 related disease

Trial contacts and locations

1

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Central trial contact

Christoph Schmaderer, M.D.; Philipp Moog, M.D.

Data sourced from clinicaltrials.gov

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