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Use of Cold and Compression Therapy With Total Knee Replacement Patients

Osteoarthritis Clinical Trial

Official title:
Investigating the Use of a Cryopneumatic Therapy Device in Primary Total Knee Arthroplasty Patients

Clinical Trial Summary

The purpose of the study is to evaluate the effectiveness of a device that delivers cold and intermittent compression as compared to ice and compressive wraps on patients who have undergone knee replacement.

Clinical Trial Description

The use of cryotherapy with compression for orthopedic postoperative recovery has not been fully investigated. A new device has been developed that combines cold and intermittent pneumatic compression in a single system. A well-controlled clinical study evaluating the clinical effectiveness of cryotherapy with compression in an orthopedic postoperative application is the subject of this protocol. Patients diagnosed with osteoarthritis of the knee and scheduled for primary total knee arthroplasty procedure will be invited to participate in this study. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00712816
Study type Interventional
Source CoolSystems, Inc.
Contact
Status Active, not recruiting
Phase Phase 4
Start date July 2008
Completion date May 2012
View Details
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