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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00785070
Other study ID # PROSPECT
Secondary ID
Status Completed
Phase Phase 4
First received November 4, 2008
Last updated February 5, 2009
Start date April 2008
Est. completion date February 2009

Study information

Verified date February 2009
Source Memorial Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

- 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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Memorial Health System Colorado Springs Colorado

Sponsors (2)

Lead Sponsor Collaborator
Memorial Health System Nexan Inc

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of objective sleep data to standardized sleep questionnaires Pre and Post Operative Yes
Secondary Compare Pre and Post Operative Objective sleep data Pre and post operative Yes
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