Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2000 participants
OBSERVATIONAL
1998-01-31
1999-01-31
Brief Summary
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Detailed Description
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1. to identify the demographic, clinical, and functional status variable that predict the risk of death, morbid events (e.g., the development of new complications or deterioration of existing conditions), or the deterioration in functional status using a half of the cohort chosen at random;
2. to combine these findings into a prognostic scale that can be employed in routine clinical practice; and
3. to validate the performance of this scale in the second half of the cohort.
There are no interventions in this study. Patients already under medical care by Cornell physicians will be enrolled. The only requirements for patients are to complete the questionnaires on an annual basis.
Conditions
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Interventions
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There are no interventions in this study
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
2. Patients who are not able to provide informed written consent.
18 Years
ALL
No
Sponsors
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Weill Medical College of Cornell University
OTHER
Responsible Party
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Weill Cornell Medical College
Principal Investigators
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Mary E Charlson, MD
Role: PRINCIPAL_INVESTIGATOR
Weill Medical College at Cornell University
Locations
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New York Presbyterian Hospital-Weill Cornell Medical College
New York, New York, United States
Countries
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Other Identifiers
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0397-727
Identifier Type: -
Identifier Source: org_study_id
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