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Clinical Trials: Orthopaedics


Source: Johannes Gutenberg University Mainz
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. Read More
Last Updated: 06 Sep 2016
Source: OAD Orthopaedics
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. Read More
Last Updated: 09 Jun 2013
Source: Arthrex, Inc.
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. Read More
Last Updated: 10 Sep 2014
Source: Rothman Institute Orthopaedics
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. Read More
Last Updated: 29 Mar 2011
Source: Stryker Orthopaedics
The purpose of this study is to evaluate clinical and radiographic outcome data in patients implanted with the Accolade® TMZF® femoral stem. Read More
Last Updated: 12 Jul 2016
Source: DePuy Orthopaedics
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. Read More
Last Updated: 24 Jul 2016
Source: Stryker Orthopaedics
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. Read More
Last Updated: 28 Nov 2016
Source: Stryker Orthopaedics
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. Read More
Last Updated: 28 Nov 2016
Source: Stryker Orthopaedics
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. Read More
Last Updated: 28 Dec 2016
Source: DePuy Orthopaedics
This study is a clinical evaluation of survivorship of an acetabular cup system after total hip replacement using patient examinations and questionnaires. Read More
Last Updated: 27 Jul 2014
Source: DePuy Orthopaedics
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. Read More
Last Updated: 26 Jan 2017
Source: Tornier, Inc.
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. Read More
Last Updated: 08 Sep 2016
Source: OAD Orthopaedics
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
Last Updated: 09 Jun 2013
Source: Rothman Institute Orthopaedics
This is a prospective, randomized control trial evaluating the efficacy of iodophor-impregnated adhesive drapes for reducing bacterial count in hip surgery. Read More
Last Updated: 27 Sep 2016
Source: Rothman Institute Orthopaedics
To collect medium to long-term survivorship implant outcomes on the DePuy Delta Xtend Reverse Shoulder Stystem. Read More
Last Updated: 16 Dec 2013
Source: Rothman Institute Orthopaedics
The purpose of this study is to correlate functional outcomes and perioperative complications with tourniquet use during total knee arthroplasty. Read More
Last Updated: 18 Sep 2016
Source: Rothman Institute Orthopaedics
This study aims to investigate short-term outcomes following the use of two femoral stems used during Total Hip arthoplasty: the Fitmore Femoral stem and the M/L Taper Femoral stem. Read More
Last Updated: 07 Apr 2013
Source: Rothman Institute Orthopaedics
This study will investigate the efficacy of using cell saver during bilater total hip arthroplasty Read More
Last Updated: 07 Nov 2011
Source: Rothman Institute Orthopaedics
The purpose of this study is to evaluate the role of new barbed suture for closure of wound during total hip arthroplasty in reducing the risk for wound healing problems. Read More
Last Updated: 17 Nov 2015
Source: Rothman Institute Orthopaedics
A non-blinded randomized controlled trial, in which participants undergoing primary reverse or total shoulder arthroplasty are randomly assigned to one of two treatment groups. Read More
Last Updated: 23 Feb 2016
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