Hospital Outcomes: Intervention in Moderately III Patients

Completed · Not applicable

Conditions studied: Moderately Ill Medical Inpatients at the Cornell Campus of the New York-Presbyterian Hospital

In brief

To evaluate the utility of real time prognostic data (illness severity, stability and function) in the improvement of hospitalization morbidity, mortality, iatrogenic complications and length of stay.

Key facts

Study ID

NCT00256659

Run by

Weill Medical College of Cornell University

People needed

444

Starts

1998-09-01

Expected to finish

1999-04-01

Last updated by the study team

2008-04-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All medical in-patients who are coded moderately ill with fair to poor function in the SIGNOUT program will be asked to participate in our study.
• Patients who are able to provide verbal consent for their participation will be enrolled.

You may not qualify if…

• Any patient not coded in the SIGNOUT system as moderately ill with fair to poor function.
• Patients who refuses not to participate in the study.
• Patients who are unable to give written informed consent.

Where it is running

• New York Presbyterian Hospital- Weill Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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