Expired Study
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Colorado Springs, Colorado 80909


Purpose:

- 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.


Criteria:

Inclusion Criteria: - Undergoing knee or hip total joint replacement - Answer Yes to any PROSPECT health history questions and/or score Positive on the sleep questionnaires Exclusion Criteria: - Tape Allergy - Previous Diagnosis Of Obstructive Sleep Apnea


NCT ID:

NCT00785070


Primary Contact:

Principal Investigator
Clayton B. Carr, M.D.
Memorial Health System


Backup Contact:

N/A


Location Contact:

Colorado Springs, Colorado 80909
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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