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Osteoarthritis clinical trials

View clinical trials related to Osteoarthritis.

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NCT ID: NCT02626533 Active, not recruiting - Pain Clinical Trials

Persistent Postoperative Pain and Joint Stiffness After Total Knee Arthroplasty Performed for Osteoarthritis

Pain+Stiffness
Start date: December 2015
Phase:
Study type: Observational

Persistent pain and joint stiffness after surgery may interfere with recovery and adversely affect quality of life in up to 40% of patients who have undergone total knee arthroplasty. There is growing evidence that inflammation as well as other medical and psychological factors may be associated with osteoarthritis severity, progression, and associated pain severity. This study aims to identify clinical, biological, and psychological factors that contribute to and predict the development of these complications. Identification of such factors may allow us to target preventative measures to the patients at highest risk of persistent postoperative pain and joint stiffness.

NCT ID: NCT02625727 Active, not recruiting - Physical Activity Clinical Trials

Effects of Hyaluronic Acid vs. Hyaluronic Acid on Knee Osteoarthritis

Start date: August 2015
Phase: Phase 4
Study type: Interventional

Using double blind, randomized controlled design to study the immediate, short-term and intermediate-term therapeutic effects of ultrasound guided hyaluronic acid injection and hyaluronic acid combined corticosteroid injection to patients with knee osteoarthritis.

NCT ID: NCT02620462 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Wearable Sensor-based Balance Training for Patients With Knee Osteoarthritis

Start date: February 2015
Phase: N/A
Study type: Interventional

Knee osteoarthritis (KOA) is one of the leading causes of lower limb disability among the elderly and can cause loss of knee joint proprioception that contributes towards deterioration of postural balance. Maintaining a good postural stability is essential while performing everyday functional activities and to avoid falls. Exercise training has been reported to reduce pain as well as improve performance of functional tasks in patients with KOA however compliance to exercise can be challenging due to pain, lack of motivation and traditional nature of exercise that can easily overtax patients. Furthermore, there are not exercise programs that are specifically designed for patients with KOA in order to address lost knee joint proprioception. Recent studies have also demonstrated that visual feedback during exercise can enhance the benefits of exercise training. Therefore, the aim of the proposed study is to implement an interactive sensor-based exercise training to improve postural balance, gait and activities of daily living in patients with KOA.

NCT ID: NCT02607579 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Comparing Exparel & Ropivacaine for Pain Relief in Total Knee Arthroplasty

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this prospective study is to examine the effect of two local anesthetics used in adductor canal blocks, with relation to pain, analgesic consumption, mobility, and pain related interference with activities and hospital length of stay. The two agents are bupivacaine and ropivacaine. The purpose of this trial is to examine the effect of these drugs being used in adductor canal blocks for pain relief, analgesic consumption, mobility, and pain related interference with activities and hospital length of stay.

NCT ID: NCT02566473 Active, not recruiting - Osteoarthritis Clinical Trials

FORCE-TJR: Improving Orthopedic Outcomes Through a National TJR Registry

FORCE-TJR
Start date: April 2011
Phase:
Study type: Observational [Patient Registry]

Aim 1. Establish a national registry of diverse patients of orthopedic surgeons representing all regions of the country and varied hospital and surgeon practice settings (e.g., urban/rural, low and high volume) to ensure that registry analyses and research reflect typical clinical practice thereby providing optimal guidance for patients, clinicians, and national healthcare policymakers. Collect pre-operative and post-operative patient reported outcomes (PROs) for pain and function. Aim 2: Develop new and transformative comparative effectiveness tools useful to both clinical practice and healthcare policy. Aim 3. Broadly disseminate surveillance reports for adverse events, such as implant revision, hip dislocation, knee manipulation, and identify important variation to inform quality improvement priorities.

NCT ID: NCT02565160 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Analysis of Human Knee Joint Fluid Using Metabonomic, Genomic and Tribology Techniques

Start date: October 2015
Phase:
Study type: Observational

Making the diagnosis underlying a painful, swollen joint currently involves aspiration followed by numerous microbiological and biochemical laboratory tests. This can be costly, time consuming and in the case of an acutely swollen joint, lead to a lengthy inpatient admission. There is an unmet need to provide a quick, easy, reliable dipstick like test to analyse joint fluid in the community, clinic, or emergency department setting. The investigators aim to use well established metabonomic techniques to: 1. Analyse fluid from patients with swollen joints 2. Identify potential biomarkers of inflammatory, infective and osteoarthritic causes of joint swelling 3. Correlate this with lubrication and wear properties of the fluid The long term goal is to develop time saving, cost effective, non-invasive diagnostic tests to improve management of a swollen joint. The biomedical research centre at Imperial provides a unique and unparalleled clinical and scientific environment to conduct this research. The Imperial College division of Computational and Systems Medicine has an international reputation in metabonomics and this, together with the high volume of patients with swollen joints treated at Imperial National Health Service Trust (c1000/yr) ensures that the study can take place in an environment conductive to success.

NCT ID: NCT02543489 Active, not recruiting - Clinical trials for Osteoarthritis of the Knee

Flex Intramedullary Rod Study

Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of post-operative ROM between Flex IM rod and Rigid IM rod, to collect bone morphology of Japanese lower extremity and to research the incidence of overhung with Flex IM rod.

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: NCT02539095 Active, not recruiting - Osteoarthritis Clinical Trials

Efficacy of Intra-articular Collagen Injection in Patients With Knee Joint Pain Compared to Normal Saline Injection

Start date: April 2014
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to confirm the superiority of intra-articular collagen injection in patients with knee joint pain compared to the control group. 100mm VAS is used to measure the pain of the subjects 24 weeks after the procedure.

NCT ID: NCT02539069 Active, not recruiting - Osteoarthritis Clinical Trials

The Post-marketing Surveillance to Evaluate the Efficacy of CHONDRON (Autologous Cultured Chondrocyte) by Arthroscopy

Start date: August 2012
Phase: Phase 4
Study type: Interventional

A clinical trial to evaluate the long-term efficacy and safety of Chondron (Autologous cultured Chondrocyte) administered through arthroscopy from the drug's 48 weeks efficacy and safety evaluation with 96 weeks follow-up in patients with knee cartilage defects.