Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Zimmer Biomet
Randomized Controlled Study to compare clinical and patient reported outcomes of the Vanguard XP Bicruciate Total Knee System to the Vanguard CR Knee System through 10 years of follow-up.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
cemented application of components
bilateral subjects randomized by knee
patients with pre-existing contralateral knee surgery
painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, or traumatic arthritis where one or more compartments are involved
correction of varus, valgus, or posttraumatic deformity
sufficient soft tissue surrounding the knee, including the Anterior Cruciate Ligament
You may not be if
cementless application of components
BMI greater than or equal to 40
use of Anterior Stabilized Bearings
patients with severe pre-operative varus or valgus deformity greater than or equal to 15 degrees
correction or revision of previous joint replacement procedure on index knee
infection
sepsis
osteomyelitis
uncooperative patient or patient with neurological disorders who is incapable of following directions
osteoporosis
metabolic disorders which may impair bone formation
osteomalacia
distant foci of infections which may spread to the implant site
rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram
