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Knee Osteoarthritis clinical trials

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NCT ID: NCT04040764 Recruiting - Knee Osteoarthritis Clinical Trials

Uncemented Tritanium TKR vs Cemented Triathlon TKR

Start date: October 15, 2019
Phase: N/A
Study type: Interventional

The Study aims to investigate whether there is a clinically important difference in peri-articular bone mineral density (BMD) and trabecular bone score (TBS) between patients undergoing two different types of knee replacement fixation - uncemented Tritanium total knee replacement (TKR) and cemented Triathlon TKR. Before undertaking a full randomised control trial however, it is necessary to establish that the proposed methodology and approach are feasible. Therefore an internal pilot study will be performed first. This registration is for the internal pilot study.

NCT ID: NCT04019782 Recruiting - Knee Osteoarthritis Clinical Trials

Collagen-PVP vs Hylan G-F 20 in the Treatment of Knee Osteoarthritis

Start date: August 1, 2019
Phase: Phase 3
Study type: Interventional

Articular cartilage degradation is the main characteristic of osteoarthritis (OA), involving enzymatic and inflammatory mechanisms that change it into a chronic disease. Since articular cartilage shows limited regenerative ability, several intra-articular drugs have been developed in order to decrease inflammation and provide a better clinical outcome to the patient.

NCT ID: NCT04017403 Recruiting - Knee Osteoarthritis Clinical Trials

Probiotics Attenuate Postoperative Cognition Decline

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate whether perioperative probiotics can reduce the incidence of postoperative cognitive dysfunction and postoperative delirium.

NCT ID: NCT04006314 Recruiting - Knee Osteoarthritis Clinical Trials

Platelet Rich Plasma and Neural Prolotherapy Injections in Treating Knee Osteoarthritis

Start date: September 4, 2018
Phase: N/A
Study type: Interventional

Osteoarthritis (OA) of the knees is the most common degenerative disorder seen in a rehabilitation outpatient clinic. It is characterized by metabolic, biochemical, and structural changes in the articular cartilage and the surrounding tissues. Knee OA patients are often troubled with knee pain and functional disturbance. Several studies have shown that the earlier the injection of autologous platelet rich plasma (a PRP) to treat early stages of knee OA, the better the treatment outcome. However, no consensus has been reached as to whether PRP injection is beneficial for patients with moderate to severe degrees of knee OA. Studies have also shown that the application of neural prolotherapy (NPT) to the genicular nerves may have beneficial effects in treating patients with severe knee OA. However, patients may start to walk for a longer period of time due to reduced knee pain after NPT. If the regenerative effect of PRP is not yet obvious on the knee cartilage, this excess walking may result in further destruction of the knee joints. No studies have examined the combined treatment effect of a PRP and NPT on patients with moderate to severe degrees of knee OA. NPT is the injection of low percentage dextrose water (5%) with the rationale to repair and reduce pain caused by the nerves. We would like to bring our PRP study to a higher level by conducting a two-year study to recruit patients with moderate to severe degrees of knee OA. PRP will be injected into the knee joint and the pes anserine tendons. Simultaneous NPT will also be performed to the genicular nerves. The effectiveness will be examined using proteomics, isokinetic measurements and functional scale evaluations. Synovial fluid (SF) is in direct contact with the cartilage and synovium, protein biomarkers related to the disease pathophysiology of knee OA are contained within the SF and will be used for proteomic analysis. Patients will receive monthly injections for a total of 3 months. In short, if inflammatory proteins in the SF are not reduced after PRP injections, this indicates that PRP is not a good treatment choice for patients with moderate to severe degrees of knee OA. If inflammatory protein concentrations are further increased after NPT as patients may start strenuous exercises with reduced knee pain, more knee joint destruction may result.

NCT ID: NCT03998943 Recruiting - Knee Osteoarthritis Clinical Trials

NOCTURNAL PAIN After Knee Arthroplasty : Incidence and Risk Factor: an Observational Study

NOCTURN-PAIN
Start date: May 6, 2019
Phase:
Study type: Observational

In prosthetic knee surgery, there is a certain number of patients with post-operative nocturnal pain. The purpose of our study is to determine the impact of this problem and to better understand its risk factors.

NCT ID: NCT03962270 Recruiting - Knee Osteoarthritis Clinical Trials

Effect of Extracorporeal Shock Wave in the Treatment of Knee Osteoarthritis

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

In this study, the effectiveness of ESWT in the treatment of knee OA was investigated from the perspective of cartilage injury,and to prove that shockwave could delay the early and middle stage OA progression by improving cartilage condition

NCT ID: NCT03955497 Recruiting - Knee Osteoarthritis Clinical Trials

Effectiveness of Autologous Adipose-derived Stem Cells in the Treatment of Knee Cartilage Injury

Start date: October 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This study was aimed to evaluate the efficacy and safety of Autologous Adipose-derived Mesenchymal Stem Cell Gel combine with High tibial osteotomy therapy in the treatment of cartilage damage in the knee. Investigator believe that this method will enable patients to recover better knee function and more repair of knee cartilage.

NCT ID: NCT03953846 Recruiting - Knee Osteoarthritis Clinical Trials

NUsurface Implant Registry

NIR
Start date: June 1, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this active post-market surveillance clinical registry study is to further characterize the therapeutic effect, the long-term safety and effectiveness of the NUsurface® meniscus implant in the real-world post-marketing setting

NCT ID: NCT03918681 Recruiting - Knee Osteoarthritis Clinical Trials

Gait Retraining Enhances Athletes' Technique

GREAT
Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The participant population for this study will be a convenience sample of 40 active duty soldiers and cadets at West Point, New York (NY) who are recovering from anterior cruciate ligament reconstruction (ACLR) and are cleared to return to run by their medical provider. Two groups will be utilized in this pre-test, post-test, single-blind randomized controlled trial study design. The purpose of this study is to determine if patients recovering from ACLR benefit from running gait retraining to adopt a forefoot strike pattern and 5-10% increase in step rate when compared to a traditional walk to run program.

NCT ID: NCT03915522 Recruiting - Knee Osteoarthritis Clinical Trials

Adductor Canal Block in an Enhanced Recovery Program After Total Knee Arthroplasty

Start date: May 14, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effectivity of adductor canal block performed the day after total knee arthroplasty surgery in reducing pain and improving walking ambulation ability and muscle strength.