Pre and Post Orthopedic Surgery Sleep and Cardiac Testing (PROSPECT)

Completed

Conditions studied: Obstructive Sleep Apnea

In brief

* Evaluate sleep disordered breathing before and after orthopedic surgery utilizing a FDA cleared to market (510k) home sleep study device (Nexan Inc., ClearPath System) * Compare Berlin Questionnaire and Epworth Sleep Scale questionnaires to the home sleep study device results. * Evaluate effectiveness of the home sleep study testing in the orthopedic presurgical population.

Key facts

Study ID

NCT00785070

Run by

Memorial Health System

People needed

100

Starts

2008-04-01

Expected to finish

2009-02-01

Last updated by the study team

2009-02-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Undergoing knee or hip total joint replacement
• Answer Yes to any PROSPECT health history questions and/or score Positive on the sleep questionnaires

You may not qualify if…

• Tape Allergy
• Previous Diagnosis Of Obstructive Sleep Apnea

Where it is running

• Memorial Health System — Colorado Springs, Colorado, United States

Full record on ClinicalTrials.gov

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