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Predicting Favorable Outcomes in Hospitalized Covid-19 Patients

Predicting Favorable Outcomes in Hospitalized Covid-19 Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04570488
Enrollment
1415
Registered
2020-09-30
Start date
2020-05-15
Completion date
2021-12-07
Last updated
2022-12-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adverse Event, Corona Virus Infection, COVID

Brief summary

Testing use of predictive analytics to predict which COVID-19+ patients are at low risk for an adverse event (ICU transfer, intubation, mortality, hospice discharge, re-presentation to the ED, oxygen requirements exceeding nasal cannula at 6L/Min) in the next 96 hours

Detailed description

To assess if display of low risk of adverse event in EPIC can safely reduce length of stay and plan for discharge.

Interventions

OTHEREPIC risk score display

Display of risk score/ colored flag in Epic patient list column

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Adult hospitalized COVID19+ patients predicted to have no adverse event at 96 events with a threshold at 90% PPV, with at least one low risk during their admission who are discharged alive and have not been in the ICU

Exclusion criteria

Age \< 18 years not hospitalized for COVID19+.

Design outcomes

Primary

MeasureTime frameDescription
Reduction in days from first low-risk score to discharge96 HoursReduction in days from first low-risk score to discharge

Secondary

MeasureTime frameDescription
Reduction in length of stay (LOS)96 hoursReduction in LOS for green patients that have not been in the ICU
Reduction in GTD vs. LOS96 hoursReduction in GTD vs. LOS for all green patients discharged alive vs all patients discharged alive
No change in 30 day re-ED presentation or hospital admission rate for cohort96 hoursNo change in 30 day re-ED presentation or hospital admission rate for cohort

Other

MeasureTime frame
Re-presentation to ED96 hours
Readmission to hospital96 hours
Mortality96 hours
Postdischarge mortality96 hours

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026