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The Short Form-36: Pre- Versus Post-Surgical Administration in Cardiac Surgery Patients

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Mary E. Charlson, MD, Weill Medical College of Cornell University
ClinicalTrials.gov Identifier:
NCT00226265
First received: September 14, 2005
Last updated: February 17, 2017
Last verified: February 2017
September 14, 2005
February 17, 2017
January 1999
December 2006   (Final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00226265 on ClinicalTrials.gov Archive Site
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The Short Form-36: Pre- Versus Post-Surgical Administration in Cardiac Surgery Patients
The Short Form-36: Pre-vs. Post-Surgical Administration in Cardiac Surgery Patients
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.
Observational
Observational Model: Case-Only
Time Perspective: Prospective
Not Provided
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Non-Probability Sample
Cardiac Surgery Patients at New York Presbyterian Hospital-Weill Cornell Medical College
  • Coronary Artery Bypass Grafting
  • Heart Diseases
  • Heart Valve Diseases
Not Provided
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
September 2007
December 2006   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
18 Years to 100 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00226265
1203-069
No
Not Provided
Plan to Share IPD: No
Plan Description: No Plan to Share IPD
Mary E. Charlson, MD, Weill Medical College of Cornell University
Weill Medical College of Cornell University
Not Provided
Principal Investigator: Mary E Charlson, MD Weill Medical College of Cornell University
Weill Medical College of Cornell University
February 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP