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Controlled Study of Kneehab XP for Patients Undergoing Total Knee Replacement

Total Knee Replacement Clinical Trial

Official title:
A Randomised Controlled Study To Compare the Effects of a Standard Therapy Protocol With a 12-week Peri-Operative Program of Kneehab XP Compared to a Control Treatment in Patients Undergoing Total Knee Replacement

Clinical Trial Summary

The study is a prospective, randomized, double-blind sham study of TKA patients who receive a standard peri-operative treatment program plus Kneehab XP versus a standard peri-operative treatment program plus a sham device.

Clinical Trial Description

The study is a double-blind randomized controlled clinical trial of approximately 118 patients (males and females) who are at least 40 years of age, who are scheduled for Total Knee Arthroplasty (TKA) surgery will be randomized into 1) a treatment group who receive Kneehab XP and a standard rehabilitation program and 2) a control group who receive only a sham device and a standard rehabilitation program. Patients are tracked for measures of function, pain, quality of life, physical performance and acceptable states status at 6 weeks and 1 week before surgery and 3, 6, 12, and 52 weeks following surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01548040
Study type Interventional
Source Theragen Inc.
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date October 2016
View Details
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