Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients

Status unconfirmed · Not applicable

Conditions studied: Flexion Contracture

In brief

The purpose of this study is to evaluate the effect of the KneeMD subject-controlled knee rehabilitation device on the incidence of postoperative flexion contracture.

Key facts

Study ID

NCT02638480

Run by

Anne Arundel Health System Research Institute

People needed

100

Starts

2015-11-01

Expected to finish

2019-04-01

Last updated by the study team

2019-02-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Measurable Knee Flexion Contracture, with deficit limiting Active Range of Motion (AROM) and Passive Range of Motion (PROM) by at least - 10°
• 18 years of age and older
• Able to understand informed consent and willingness to conform to trial responsibilities

You may not qualify if…

• Previous surgical treatment of knee, including tibial osteotomy
• Botulinum Toxin Treatment within the last four months
• Mechanical joint impingement
• Neuromuscular pathologies such as epilepsy
• Treatment with quinolone, antibiotic medication
• Pregnant or nursing
• Fractures
• Osteomyelitis or any orthopedic infection
• Extensor mechanism dysfunction
• Knee joint neuropathy
• Previous Stroke or Brain Injury

Where it is running

• Anne Arundel Medical Center — Annapolis, Maryland, United States

Full record on ClinicalTrials.gov

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