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OpenTrials
Completed

NCT Number: NCT00922168

Pre-operative Polysomnography Assessment of Cardiac Surgery Inpatients

The purpose of this study is to assess the prevalence and morbidity rates of sleep disordered breathing in cardiac surgery patients.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects undergoing major cardiovascular surgery (coronary artery bypass graft, valve replacement surgery, or aortic surgery) under general anesthesia.
  • Subjects in whom surgery is planned for greater than 1 day but less than 60 days from the time of enrollment.

Exclusion criteria

  • Subjects treated for sleep apnea with positive airway pressure (PAP) therapy or oral appliance in the past 30 days.
  • Subjects undergoing Maze procedure for atrial fibrillation.
  • Subjects unable to comply with study procedures.

Treatment and study plan

Primary outcomes

  1. Prevalence of Sleep Disordered Breathing in Cardiac Surgery Patients

    Time frame: September 2009

Secondary outcomes

  1. Assess Post-Operative Complications of Patients with Sleep Disordered Breathing

    Time frame: September 2009

Sponsors and collaborators

Lead sponsor

Cleveland Medical Devices Inc

Industry

Collaborators

  • Johns Hopkins University
  • National Institutes of Health (NIH)
  • The Cleveland Clinic

Registry information

Official study title

Pre-operative PSG Assessment of Cardiac Surgery Inpatients

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Jun 17, 2009
Registry last updated
Feb 6, 2014

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.

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