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NCT00226265 Clinical Trial

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

Heart Diseases Clinical Trial

Official title:
The Short Form-36: Pre-vs. Post-Surgical Administration in Cardiac Surgery Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00226265
Other study ID # 1203-069
Secondary ID
Status Completed
Phase N/A
First received September 14, 2005
Last updated February 17, 2017
Start date January 1999
Est. completion date September 2007

Study information
Verified date February 2017
Source Weill Medical College of Cornell University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date September 2007
Est. primary completion date December 2006
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States The New York Presbyterian Hospital-Weill Medical Center New York New York

Sponsors (1)
Lead Sponsor Collaborator
Weill Medical College of Cornell University

Country where clinical trial is conducted

United States, 

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