The Short Form-36: Pre- Versus Post-Surgical Administration in Cardiac Surgery Patients
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ClinicalTrials.gov Identifier: NCT00226265
Recruitment Status :
First Posted : September 26, 2005
Last Update Posted : February 23, 2017
Weill Medical College of Cornell University
Information provided by (Responsible Party):
Mary E. Charlson, MD, Weill Medical College of Cornell University
The purpose of this study is to determine whether the SF-36 can be administered reliably to cardiac surgery patients (two to three days) post-surgery, with the patient answering the questions of this survey from a pre-surgical perspective.
The purpose of this study, is to determine whether the SF-36 can be administered reliably to cardiac surgery patients (two to three days) post-surgery, with the patient answering the questions of this survey from a pre-surgical perspective.
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Layout table for eligibility information
Ages Eligible for Study:
18 Years to 100 Years (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Cardiac Surgery Patients at New York Presbyterian Hospital-Weill Cornell Medical College
Cardiac surgery patients who are between the ages of 18 and 100
Are English speaking
Able to give consent
Undergoing cardiac surgery including (but not limited to):