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

Memorial Health System

Status: Completed

Conditions: Obstructive Sleep Apnea

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00785070

PROSPECT

Details and patient eligibility

About

• 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.

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

100 participants in 1 patient group

1

Description:

Perioperative