About this trial
This study utilizes physiological indicators of COVID-19 patients as tools for assessing, tracking, worsening, and improving the clinical symptoms of COVID-19 patients. This study employs simple and easy-to-use assessment methods, which can be further aided by artificial intelligence technology to facilitate early response and medication.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Reviewing the patient's medical history, the primary focus was on hospital records and existing physiological parameters such as blood pressure, heart rate, respiratory rate, and level of consciousness. The patient received treatment at the hospital between May 2022 and March 2027
Disqualifiers
Excluding patients with incomplete clinical data or missing information in their medical records.
Trial population
The COVID-19 patient received treatment at the hospital between May 2022 and March 2027 from emergency room, OPD
Trial design
Case-control
Retrospective
Treatments tested in this trial
physiological parameters
Other interventionsystolic blood pressure, diastolic blood pressure , heart rate, respiratory rate , GCS
Treatment groups
Trial outcomes
Primary outcomes
Shock index(SI) in the management of COVID -19
SI= heart rate / systolic blood pressre
Mordified shock index(MSI) in the management of COVID -19
MSI=heart rate / mean arterial pressure
Age shock index(Age SI) in the management of COVID -19
Age shock index =Age x (heart rate / systolic blood pression)
Respiratory adjusted shock index (RASI) in the management of COVID-19
Respiratory adjusted shock index =(heart rate/systolic blood pression) x (repiratory rate/10)
Sponsors and contacts
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