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

NCT00785070 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2009-02-09

No results posted yet for this study

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.

Conditions

Sponsors & Collaborators

  • Nexan Inc

    collaborator INDUSTRY

  • Memorial Health System

    lead OTHER

Principal Investigators

  • Clayton B. Carr, M.D. · Memorial Health System

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2009-01-31
Completion
2009-02-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00785070 on ClinicalTrials.gov