The aim of the study is to compare fracture healing, quality of life, pain, and cost of care
of the use of CERAMENT™|BONE VOID FILLER as bone graft substitute to the use of autologous
cancellous bone graft (iliac crest) in the treatment of patients with tibia fractures
treated by internal fixation and void reconstruction.
The primary objective of this pilot study is to determine the precision of post-operative
radiostereometric measurements for the assessment of lumbar spinal fusion. This study will
also determine the potential for RSA as a more precise and accurate means for assessment of
lumbar spinal fusion and diagnosis of pseudarthrosis.
The purpose of this study is to establish an international, web based clinical registry to
collect baseline characteristics of patients undergoing orthopaedic, sports medicine,
arthroscopy, and related surgery, and the subsequent outcomes and cost-effectiveness
associated with the surgical procedures and nonoperative treatments.
Metaphyseal sleeves, through their design, could allow reconstruction of the knee in cases
of severe bone loss by allowing rigid internal fixation and proper alignment of the
extremity and components.
This study is designed to compare the surgical efficiency of TruMatch® Personalized
Solutions surgical technique compared to conventional surgical technique. Specifically, the
purpose of this study is to collect time data to enhance the existing economic model.
The purpose of this study is to evaluate the clinical outcomes (range of motion, pain,
function, radiographic stability, and health related quality of life) of patients receiving
the Triathlon® Posterior Stabilized (PS) Total Knee System. These outcomes will be evaluated
using pre-operative scores and comparing them to post-operative scores in addition to being
compared with cases who received the Scorpio® PS implant.
The primary objective of the study is to demonstrate the linear wear rates of the Trident®
X3 polyethylene insert are superior to a polyethylene control group wear rate at 5 years
postoperative. This measurement will be evaluated by comparing digitized images of serial
radiographs obtained over a follow-up period of 5-years.
This study will be an evaluation of the Rejuvenate® Modular Hip System for primary total hip
replacement (THR) with a cementless application in a consecutive series of patients who meet
the eligibility criteria. Subjects will be evaluated for freedom of hip revision at 5 years
and clinical outcomes for up to 10 years after surgery.
This registry is intended to evaluate the clinical outcomes of the DePuy P.F.C. Sigma PS150
RP Total Knee System. 200 participants will be enrolled prospectively or retrospectively and
the follow up period will be 5 years. Data collection will include Radiographic Analysis,
Knee Society Evaluation and Adverse Events.
The Tornier Shoulder Outcomes Study is designed to collect safety and efficacy data on
designated commercially available Tornier Shoulder repair products. In addition, this study
will provide performance data for use in education, marketing materials, peer-reviewed
publications and support research and development of future products.
The optimal surgical treatment for insertional Achilles tendinopathy remains unclear. The
purpose of this study is to evaluate the long-term outcome of surgical treatment by
comparing the patient reported outcomes of Insertional Achilles Tendinopathy; Achilles
tendon debridement, excision calcaneal exostosis, Strayer procedure, secondary repair of
Achilles with flexor hallucis longus (FHL) transfer and Achilles tendon debridement,
excision calcaneal ... Read More