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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02386254
Other study ID # ECOG 9058
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date November 26, 2018
Est. completion date November 18, 2019

Study information

Verified date March 2024
Source University of Oklahoma
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate whether a premorbid functioning scoring system such as the ECOG system can be adapted to predict ICU morbidity and mortality.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 18, 2019
Est. primary completion date November 18, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients aged 18 years and older admitted to the Presbyterian Hospital intensive care units under the medical ICU service. Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States OU Medical Center Oklahoma City Oklahoma

Sponsors (1)

Lead Sponsor Collaborator
University of Oklahoma

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 30-day
See also
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