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Completed

NCT Number: NCT00226265

The Short Form-36: Pre- Versus 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.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The New York Presbyterian Hospital-Weill Medical Center

New York, 10021, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Sponsors and collaborators

Lead sponsor

Weill Medical College of Cornell University

Other

Registry information

Official study title

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

Important dates

Study start
1999
Primary completion
2006
Study completion
2007
First posted
Sep 26, 2005
Registry last updated
Feb 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.