An observational study in ICU Mortality and ICU Morbidity, sponsored by University of Oklahoma. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-12.
Sponsored by University of Oklahoma · Observational
To evaluate whether a premorbid functioning scoring system such as the ECOG system can be adapted to predict ICU morbidity and mortality.
University of Oklahoma is the lead sponsor of 424 studies on the registry; 99 are open to participants now.
Of its 42 completed or terminated interventional studies of FDA-regulated products, 16 (38%) have results posted.
Counted across the registry records on this site, refreshed daily.
Patients admitted to the critical care units of Presbyterian Hospital under the care of the medical ICU service with any diagnosis will be assessed for enrollment.
Exclusion Criteria:
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Mortality
Data will be expressed as mean + SD. Non parametric data will be expressed as median with interquartiles. Student t-test will be used to compare the normally distributed data, and the Mann-Whitney U test will be used for non parametric data. Chi-Squared test will be used to assess for trend between the ECOG score and the 30-day mortality. The investigators will use logistic regression analysis to determine the factors (including the ECOG score) associated with the 30-day mortality. Significance will be accepted for p values \< 0.05.
Time frame: 30-day
This study is withdrawn, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.
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University of Oklahoma