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Osteoarthritis, Knee clinical trials

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NCT ID: NCT03289754 Terminated - Knee Osteoarthritis Clinical Trials

A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial Inserts

Start date: January 24, 2018
Phase: N/A
Study type: Interventional

This study is designed to evaluate the clinical outcomes of subjects who have recently undergone surgery with the iTotal® Cruciate Retaining (CR) Total Knee Replacement System (KRS) who have also had iPoly XE Tibial Inserts implanted.

NCT ID: NCT03275246 Terminated - Knee Osteoarthritis Clinical Trials

Establish Implant Accuracy With X-PSI Knee System

X-PSI
Start date: October 5, 2018
Phase: N/A
Study type: Interventional

The goal of this study is to establish the accuracy of the new X-PSI Knee System guides by analyzing early postoperative (4-6 weeks) imaging data with regards to the mechanical alignment and compare them with preoperative planning imaging data. Mechanical alignment in the hip-knee-ankle (HKA) frontal plane with X-PSI Knee System will be measured and compared with results reported in the literature using a conventional (non-guided) approach. Hypothesis: The use of the new X-PSI Knee System achieves the same accuracy with respect to mechanical alignment as with conventional instrumentation.

NCT ID: NCT03199417 Terminated - Knee Osteoarthritis Clinical Trials

Trial Evaluating multimOdal toPical Cream In CompArison to pLacebo (TOPICAL)

TOPICAL
Start date: May 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Randomized controlled trial regarding the efficacy of a multimodal topical analgesic, Multiprofen, in comparison to placebo cream treatment on knee pain and function in patients with knee osteoarthritis.

NCT ID: NCT03171168 Terminated - Knee Osteoarthritis Clinical Trials

The Effect of AposTherapy on Knee Pain

AposKnee
Start date: November 30, 2016
Phase: N/A
Study type: Interventional

AposTherapy is a home based exercise program utilizing footwear that causes exercise with normal activity that may significantly improve function in patients with knee osteoarthritis since patients with knee osteoarthritis have altered mechanics of motion contributing or due to the presence of the conditions. Capitalizing on the reported excellent adherence and clinical benefit of ApostTherapy in patients with significant knee OA, the investigators propose to evaluate this as a conservative treatment that may supplant/supplement traditional pain medications and physical therapy in an at-risk urban inner city population.

NCT ID: NCT03153956 Terminated - Clinical trials for Osteoarthritis, Knee

Efficacy of AposTherapy® in Knee OA

Start date: April 16, 2015
Phase: N/A
Study type: Interventional

A prospective, interventional, randomized, double-arm clinical evaluation study to examine the efficacy of AposTherapy® versus a control group, in the short-term at 6 months and in the long-term at 12 months post-treatment, with the primary efficacy assessment based on improvement in knee pain score and improvement in function in patients following diagnosis of knee osteoarthritis (OA).

NCT ID: NCT03153813 Terminated - Pain Clinical Trials

Capsaicin Patches In Knee Osteoarthritis In Obese Patients

CHILI-OB
Start date: July 2015
Phase: Phase 3
Study type: Interventional

To assess the efficacy and safety of high concentration capsaicin patches in pain due to osteoarthritis (OA) of the knee in patients with obesity

NCT ID: NCT03152162 Terminated - Clinical trials for Osteoarthritis, Knee

A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement System

Start date: May 1, 2017
Phase:
Study type: Observational

This is a prospective clinical study designed to observe the long-term clinical outcomes of total knee arthroplasty using a patient-specific, posterior stabilized implant in patients with osteoarthritis.

NCT ID: NCT03146819 Terminated - Clinical trials for Osteoarthritis, Knee

A Single Time-Point Study to Evaluate the ConforMIS iTotal (PS) Knee Replacement System Versus Off-the-Shelf

Start date: December 16, 2016
Phase:
Study type: Observational

This study is designed to compare outcome data for patients who have recently undergone surgery with the iTotal® Posterior Stabilizing (PS) Knee Replacement System (hereafter referred to as the "iTotal") versus those who have undergone surgery with Off-the-Shelf (OTS) systems.

NCT ID: NCT03113149 Terminated - Clinical trials for Osteoarthritis, Knee

Strongest Predictors of a Positive Outcome After Physiotherapy for Knee Osteoarthritis

Start date: May 1, 2017
Phase: N/A
Study type: Observational

Individuals with painful knee osteoarthritis (OA) experience restricted physical function. Few previous studies have investigated comprehensive sets of constructs and tests to investigate physical function in these patients. Most single studies of knee OA patients show limited scope for explaining physical function in the perspective of WHO's International Classification of Functioning, Disability and Health (ICF) 3 levels: Body functions (the bodily level), Activities (individual level), and Participation (societal level). On the bodily level there is limited case-control knowledge on muscle strength beyond the knee and endurance-strength in general. On the activity level, there is similar limitation of biomechanical bodily features in stair climbing. On the participation level the situation is similar for objective performance. Measures are needed that inter-relate all three levels of ICF. These should also include well discriminating tests e.g. knee strength, walking, and activities of daily life (ADL), as well as both objective and subjective measures. The purpose of this study is to explore mechanisms that can explain physical function in patients with knee OA in primary care. The study's main and primary goal is to quantify which baseline factors and change scores are the strongest predictors of a positive treatment outcome in terms of patients' global perceived change after physiotherapy. Secondary research question is: which factors are the strongest predictors of a positive outcome of physiotherapy in knee OA, in terms of pain intensity, patient specific functional scale, and function in daily living?

NCT ID: NCT03058393 Terminated - Knee Osteoarthritis Clinical Trials

Analyzing Challenging Clinical Discussions in Orthopaedics

Start date: April 17, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to analyze patient:provider communication surrounding the discussion of difficult clinical conversations such as knee replacement options. This study will also examine how using the teach-back communication technique can improve communication between patients and providers. Orthopedic residents, fellows, physician assistants, and attendings that agree to participate will be consented. Patients, who are likely to engage in a difficult clinical conversation, such as those who have a clinical indication for a Total Knee Replacement or a Partial Knee Replacement, will be recruited from participating providers clinical schedules. Patient:provider interactions will be recorded and then the providers will attend a 1 hour education lecture about how to use teach-back. After attending the lecture, additional patient:provider interactions will be recorded and analyzed via a qualitative approach. Additionally, providers will participate in a semi-structured interview to capture their perceptions of teach-back and what challenges and benefits they may derive from using it.