Clinical Trials Logo

Joint Diseases clinical trials

View clinical trials related to Joint Diseases.

Filter by:

NCT ID: NCT03357445 Active, not recruiting - Clinical trials for Post-Traumatic Arthritis

AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study

Start date: October 14, 2011
Phase: N/A
Study type: Interventional

This is a Post Marketing Clinical Follow Up study (PMCF) on the AVANTAGE RELOAD dual mobility system cup.

NCT ID: NCT03294408 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Multimodal Imaging of Subchondral Bone in Knee Osteoarthritis : Predictive Model

MOSART
Start date: November 29, 2016
Phase: N/A
Study type: Interventional

Predictive factors of osteoarthritis progression are not yet well understood. However, a growing role attaches importance to the subchondral bone. The aim of the present project is to determine predictive factors of progression of osteoarthritis at the knee by a multimodal characterization of subchondral bone by Medical Resonnance Imaging, direct high resolution digitization radiographs and bone texture analysis. At the end of the project, an innovative imaging device, combining semi-automatic softwares for texture analysis, control detection and image registration would be supplied. This will enable on the one hand a more accurate and reproducible way to measure the joint space width of the affected compartment and on the other hand, an assistance to better detect patients at risk of progression of their knee osteoarthritis. Identifying These "progressors" patients might permit their selection in clinical trials at baseline adapted to their severe disease, using for example biologic treatments targeting knee osteoarthritis. The main objective of this study is to analyze the predictive capacities of bone texture parameters measured on the high-resolution radiography of the knee on the structural evolution of the knee osteoarthritis at 3 years.

NCT ID: NCT03266874 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

G7 BiSpherical Acetabular Shell PMCF Study

Start date: December 10, 2017
Phase:
Study type: Observational

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for the commercially available G7 BiSpherical Acetabular Shell.

NCT ID: NCT03106129 Active, not recruiting - Pain Clinical Trials

Opioid Requirements Post Discharge of Patients Having Total Knee Arthroplasty (TKA)

Start date: February 9, 2017
Phase:
Study type: Observational

Total knee arthroplasty (TKA) may result in significant postoperative pain. The majority of these patients are prescribed opioids for the management of postoperative pain. Recent evidence has highlighted that postoperative opioids are being over-prescribed resulting in opioid misuse and abuse. Over-prescribing also results in a significant financial cost. This prospective observational study was designed to determine the mean amount of opioid required after TKA. This data can be used in the future as a guide to change our current practice of prescribing with the aim to reduce over-prescription.

NCT ID: NCT02997410 Active, not recruiting - Clinical trials for Temporomandibular Joint Disorders

Ozone Therapy for Masticatory Muscle Pain (OTMMP)

OTMMP
Start date: December 2014
Phase: N/A
Study type: Interventional

This study investigates the efficacy of bio-oxidative ozone application in the treatment of TMD of muscular origin.

NCT ID: NCT02823834 Active, not recruiting - Joint Disease Clinical Trials

PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular Components

Start date: June 16, 2017
Phase:
Study type: Observational

MicroPort Orthopedics (MPO) is conducting this post market clinical follow-up (PMCF) study to evaluate the safety and efficacy of its total hip arthroplasty (THA) components marketed in the European Union (EU). These types of studies are required by regulatory authorities for all THA devices that do not have medium to long-term clinical evidence available at the time of gaining approval to market in the EU. This study has been designed in accordance with the medial device directives (MEDDEV) 2.12/2 rev 2.

NCT ID: NCT02581605 Active, not recruiting - Arthritis of Knee Clinical Trials

Correction of Angular Deformities in Knee Arthrosis

Start date: November 2014
Phase:
Study type: Observational

For participants whose leg bones don't line up properly, extra stress is placed on either the inner or outer side of the knee joint due to uneven transfer of body-weight. Gradually, this extra pressure wears away the smooth cartilage, resulting in osteoarthritis on that side of the knee joint. This problem is particularly common in young athletes and places them at risk of early osteoarthritis. An operation exists whereby one of the bones either side of the knee is cut ( an osteotomy) and hinged open to straighten the leg. This alteration redistributes body-weight more equally across the knee joint and is known to be effective in delaying and possibly preventing, the progression of knee osteoarthritis- especially in younger and physically more active patients in whom a knee replacement is undesirable. Currently it is possible to ( accurately) calculate the precise position of the bone cut and number of degrees correction required to straighten a leg using digital x-rays and three-dimensional CT scans. However there is no method of implementing this pre-operative plan during surgery so that the majority of surgeons rely on relatively crude and ipso facto unreliable intra-operative measurements as a guide. To improve the accuracy of this operation, the investigator propose the use of a custom-made 'cutting block', tailored for each individual patient and its shape will match the contour of the patient's bone to ensure it can only be placed in one position. Pre-cut slots and holes will then guide the saw cut and the number of degrees the bone in hinged open, as per the pre-operative plan; it functions as an intra-operative template for the surgeon. This study will primarily examine whether there is a close match between the planned and actual correction of leg deformities when using a patient-matched cutting-block.

NCT ID: NCT02543437 Active, not recruiting - Clinical trials for Degenerative Joint Disease

Large Head X3 Study

Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the benefit of X3 polyethlene inserts with larger diameter heads used in the Japanese population. Range of Motion (ROM) and lift-off distance for both 28mm, 32mm and 36mm in patients will be examined intraoperatively by using the Stryker computerized tomography (CT) based Navigation system. Another aspect of this study is to observe wear resistance performance of X3 over historical liner existing highly crosslinked polyethylene.

NCT ID: NCT02537067 Active, not recruiting - Clinical trials for Defect of Articular Cartilage

Efficacy and Safety of Chondron (Autologus Chondrocyte) in Patients With Cartilage Defects in Their Ankle

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of Chondron (Autologus Chondrocyte) in patients with cartilage defects in their ankle for 18 months

NCT ID: NCT02444299 Active, not recruiting - Clinical trials for Avascular Necrosis of the Head of Humerus

Aequalis Resurfacing Head Study

Start date: April 2011
Phase:
Study type: Observational

Aequalis® Resurfacing Head implant is a range of shoulder arthroplasty device available for the treatment of various shoulder pathologies. It received CE Mark in June 2007. The aim of this study is to collect immediate medium and long term data on performance and safety of the implant, retrospectively as well as prospectively, from a consecutive series of patients to assess the patients' outcomes and functional status.