The Short Form-36: Pre- Versus Post-Surgical Administration in Cardiac Surgery Patients
This trial is active, not recruiting.
|Conditions||coronary artery bypass grafting, heart diseases, heart valve diseases|
|Sponsor||Weill Medical College of Cornell University|
|Start date||January 2000|
|End date||September 2007|
|Trial size||200 participants|
|Trial identifier||NCT00226265, 1203-069|
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.
Male or female participants at least 18 years old.
Inclusion Criteria: - 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): - Aortic valve replacement (AVR) - Mitral valve replacement (MVR) - Tricuspid valve replacement (TVR) - Coronary artery bypass graft (CABG). Exclusion Criteria: - Non-cardiac surgery patients
|Official title||The Short Form-36: Pre-vs. Post-Surgical Administration in Cardiac Surgery Patients|
|Principal investigator||Mary E Charlson, MD|
|Description||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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