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Pandemic Triage Score in Patients With Known or Suspected Severe Acute Respiratory Syndrome (SARS) CoronaVirus (CoV) 2 Infection (STC-19)

G

Groupe Hospitalier de la Rochelle Ré Aunis

Status

Completed

Conditions

Covid19
SARS-CoV-2 Acute Respiratory Disease

Treatments

Diagnostic Test: STC-19 score

Study type

Observational

Funder types

Other

Identifiers

NCT04371471
2020/P04/288

Details and patient eligibility

About

During this pandemic period, the goal of the health care system is to optimize the use of intensive care services for patients infected with SARS-CoV-2, given the frequency of complications that can lead to high mortality.

When patients with suspected or confirmed COVID-19 are admitted to hospital, whether or not they are symptomatic, there is currently no method to predict who will progress to complications requiring the use of intensive measures in 24-48 hours.

Full description

The body undergoes a systemic adaptation response to severe illness. Elevated cortisol and systemic inflammation are two key responses. Along with hypotension, this triad can lead to end-organ failure and death in critical illness. In critical illness, serum cortisol is dissociated from its tissular activity. We have developed a formula that calculates tissular action of cortisol called the cortisol index. It correlates in chronic ambulatory illness, and acute illness such as myocardial infarction (manuscript pending). Elevated neutrophil to lymphocyte ration (NLR) is a marker of systemic inflammation and predictor of mortality on admission to the emergency department. We have confirmed this in a retrospective and prospective study (manuscript pending, data available upon request).

The purpose of this study is to evaluate a triage score (STC-19) based on patients' biological state at the time of diagnosis, to objectively determine which patients are most likely to require intensive medical services within 24-48 hours of presentation of the emergency department.

Enrollment

91 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with clinical signs of CoV-2-SARS infection
  • Complete blood count test and systolic blood pressure available at the time of diagnosis
  • Informed of the study.

Exclusion criteria

  • Women beyond the 1st trimester of pregnancy
  • Persons under-the-age-of or legally-denied medical decision-making capacity by a judicial or administrative decision,
  • Persons of full age who are subject to a legal protection measure,
  • Persons unable to consent,
  • Persons who are not members of or beneficiaries of a social welfare program administered by the Republic of France
  • Patient's refusal to participate in the study.

Trial design

91 participants in 1 patient group

Patient with COVID-19
Description:
Patient with clinical signs of CoV-2-SARS infection and signs of severity
Treatment:
Diagnostic Test: STC-19 score

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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