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

Sponsor
Weill Medical College of Cornell University (Other)
Overall Status
Completed
CT.gov ID
NCT00226265
Collaborator
(none)
50
Enrollment
1
Location
104
Actual Duration (Months)
0.5
Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Detailed 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.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    50 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    The Short Form-36: Pre-vs. Post-Surgical Administration in Cardiac Surgery Patients
    Actual Study Start Date :
    Jan 1, 1999
    Actual Primary Completion Date :
    Dec 1, 2006
    Actual Study Completion Date :
    Sep 1, 2007

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 100 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      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

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 The New York Presbyterian Hospital-Weill Medical Center New York New York United States 10021

      Sponsors and Collaborators

      • Weill Medical College of Cornell University

      Investigators

      • Principal Investigator: Mary E Charlson, MD, Weill Medical College of Cornell University

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Mary E. Charlson, MD, Principal Investigator, Weill Medical College of Cornell University
      ClinicalTrials.gov Identifier:
      NCT00226265
      Other Study ID Numbers:
      • 1203-069
      First Posted:
      Sep 26, 2005
      Last Update Posted:
      Feb 23, 2017
      Last Verified:
      Feb 1, 2017
      Individual Participant Data (IPD) Sharing Statement:
      No
      Plan to Share IPD:
      No
      Keywords provided by Mary E. Charlson, MD, Principal Investigator, Weill Medical College of Cornell University
      Cardiac surgery patients
      Quality of Life
      Recall bias
      Aortic valve replacement
      Mitral valve replacement
      Tricuspid valve replacement
      Coronary artery bypass graft surgery
      Additional relevant MeSH terms:
      Heart Diseases
      Heart Valve Diseases

      Study Results

      No Results Posted as of Feb 23, 2017