Flexion Contracture Following Total Knee Replacement
Conditions
Brief summary
The goal of this research project is to evaluate injections of botulinum toxin A (Botox) as the treatment for knee flexion contracture after total knee arthroplasty (TKA). The current treatment for patients who do not achieve full extension of the knee (flexion contracture) after TKA consists of an aggressive physical therapy program, home stretching program, and the use of an extension orthosis (brace). Many patients do not tolerate wearing these braces. This initial project is designed to use injections of Botox as an adjunct to the standard current treatment and evaluate its efficacy. It is our hypothesis that a single injection into the hamstrings in addition to routine postoperative rehabilitation will result in improved knee extension and this improvement in function should endure without further treatment.
Interventions
DRUGBotox
DRUGplacebo
Sponsors
Sharpe-Strumia Research Foundation
Rothman Institute Orthopaedics
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Subject is at least 18 years of age * Subject had a total knee replacement or total knee replacement revision surgery performed at Main Line hospitals such as Bryn Mawr Hospital, Lankenau Hospital, and Riddle Hospital * Subject is measured to have at least 10 degree flexion contracture of the operative knee four to six weeks following surgery * Subject has the willingness to complete scheduled follow up evaluations as described in the informed consent
Exclusion criteria
* Subject is currently involved in another study or has received investigational product or treatment within the last 30 days * Subject is a prisoner * Subject is anticipated to be non-compliant * Subject is known to be pregnant * Subject is mentally incompetent or unable to understand what participation in the study entails * The subject has a known sensitivity or allergic reaction to Botulinum Toxin A and albumin * The subject is unwilling or unable to give consent or to comply with the follow up program
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Range of Motion: knee | 1 year |
Countries
United States
Contacts
Primary ContactTiffany Morrison, MS, CCRP
Outcome results
None listed