N/A
N=91
Pandemic Triage Score in Patients With Known or Suspected Severe Acute Respiratory Syndrome (SARS) CoronaVirus (CoV) 2 Infection
SARS-CoV-2 Acute Respiratory Disease · Covid19
Bottom Line
View on ClinicalTrials.gov: NCT04371471 ↗Enrolled (actual)
91
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcome: Primary: Number of Participants With Normal and Above Triage (STC-19) Score — 52; 12; 4; 5 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- STC-19 score (Diagnostic_test)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Groupe Hospitalier de la Rochelle Ré Aunis
- Primary completion
- Apr 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Normal and Above Triage (STC-19) Score |
52; 12; 4; 5; 0; 8 | — |
| SECONDARY Number of Participants With Normal and Above Genito-thyroid Index (GTi) Value |
33; 4; 11; 10; 12; 11 | — |
Summary
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.
Eligibility Criteria
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.
Data sourced from ClinicalTrials.gov (NCT04371471). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.