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

Memorial Health System100 enrolled

Overview

* 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.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Obstructive Sleep Apnea

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Memorial Health System

Colorado Springs, Colorado, United States

Outcomes

Primary Outcomes

Comparison of objective sleep data to standardized sleep questionnaires

Time frame: Pre and Post Operative

Secondary Outcomes

Compare Pre and Post Operative Objective sleep data

Time frame: Pre and post operative

Data from ClinicalTrials.gov

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