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Osteoarthrosis clinical trials

View clinical trials related to Osteoarthrosis.

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NCT ID: NCT05697952 Completed - Osteoarthrosis Clinical Trials

E1K Intra Articular(IA) Treatment for Knee Osteoarthritis

Start date: June 13, 2022
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of pain relief treatment on knee osteoarthritis when administered E1K or placebo in patients with knee osteoarthritis aged 40 to 70 to determine the optimal dose.

NCT ID: NCT03093038 Completed - Osteoarthrosis Clinical Trials

Early Stability of the Delta-TT Cup With Polyethylene Insert Versus a Ceramic Insert. A RSA Study.

RSA-DELTA-TT
Start date: May 2014
Phase: N/A
Study type: Interventional

The goal of this study is to study the stability of the Delta-TT cup with polyethylene insert and the Delta-TT cup with ceramic insert both combined with the H-MAX femoral stem by means of RSA to assess whether the differences in stiffness of the cup will have an influence on incorporation and mechanical stability. It is hypothesized that there will be more micromotion on the short-term (<2 years) in the patients with the ceramic insert because of the higher stiffness, however, all components will be considered stable on the short and long-term.

NCT ID: NCT02967874 Completed - Osteoarthritis Clinical Trials

Autologous Adipose-Derived Stromal Vascular Fraction Cells for Osteoarthritis Treatment

Start date: March 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Adipose-derived stromal vascular fraction cells (SVFs) include regenerative cell populations (hematopoietic cells, pericytes, endothelial cells and progenitors, stromal/stem cells) and thus are potentially important as new therapeutic tools for the repair and regeneration of acute and chronically damaged tissues. The general objective of this study is to evaluate safety and clinical efficacy of a single intra-articular injection of freshly isolated auto-SVFs for the treatment of patients with knee osteoarthritis (OA). This study uses autologous adipose-derived SVFs, as therapeutic agent and intra-articular administration, as a mode of delivery. Expected clinical effects: a treatment reduces pain, increases function and reduces stiffness in the knees of osteoarthritic subjects.

NCT ID: NCT02910830 Completed - Osteoarthrosis Clinical Trials

Osteoarthritis Relationships and Tobacco " Ancillary Study Khoala "

Start date: September 2014
Phase: N/A
Study type: Observational [Patient Registry]

The role of tobacco in osteoarthritis remains controversial. The Khoala cohort is the first multicenter French cohort of subjects with knee and / or hip osteoarthritis prevalent . It guarantees its methodology great representativeness and therefore an interesting material for the study of risk factors in the population. In addition, it should have little here Radiographs of hands for all its patients. It therefore has the opportunity to study a possible relationship between tobacco and hip osteoarthritis , knee and hand but also to study the relationship between tobacco and structural evolution of hip osteoarthritis and / or symptomatic knee.

NCT ID: NCT02542592 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Immune Signaling in Hip-arthroplasty Patients

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total hip-arthroplasty (THA) surgery. The investigators examine the effect on immune signaling and recovery after surgery. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving Methylprednisolone will experience a positive modulation of the immune response and an enhanced recovery.

NCT ID: NCT02445898 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Orthostatic Intolerance and Heart Rate Variability in Hip-arthroplasty Patients

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total hip-arthroplasty (THA) surgery. The investigators examine the effect on orthostatic intolerance, orthostatic hypotension and heart rate variability (HRV) to evaluate the efficacy of Methylprednisolone regarding blood pressure regulation and autonomic responses after THA. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving Methylprednisolone will be less orthostatic intolerant, experience less orthostatic hypotension and have an improved autonomic response compared to the placebo-group, early after THA.

NCT ID: NCT02332629 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Endothelial Function in Patients Undergoing Total Knee-arthroplasty

Start date: January 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the pathophysiological effects of a single dose methylprednisolone administered prior to total knee-arthroplasty surgery (TKA). The investigators examine the effect on the endothelial glycocalyx shedding due to surgical trauma. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving methylprednisolone will experience reduction in glycocalyx degradation compared to the placebo-group, early after TKA.

NCT ID: NCT02332616 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Complement Activation in Patients Undergoing Total Knee-arthroplasty

Start date: January 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the pathophysiological effects of a single dose of methylprednisolone administered prior to total knee-arthroplasty surgery. The investigators examine the effect on complement activation. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving methylprednisolone will experience beneficial inhibition of the undesirable parts of the complement activation.

NCT ID: NCT02332603 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Glucose Homeostasis in Patients Undergoing Total Hip- and Knee-arthroplasty

Start date: January 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the pathophysiological effects of a single dose of Methylprednisolone administered prior to total hip- and knee-arthroplasty surgery. The investigators examine the effect on blood glucose homeostasis. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the glucose homeostasis remains equally stable in the group receiving Methylprednisolone as in the group receiving placebo.

NCT ID: NCT02319343 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Quadriceps Muscle Function in Patients Undergoing Total Knee-arthroplasty

Start date: January 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total knee-arthroplasty (TKA). The investigators examine the effect on thigh muscle function to evaluate the efficacy of Methylprednisolone on knee-extension strength at discharge after TKA. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving Methylprednisolone will experience smaller loss of knee-extension strength compared to the placebo-group, early after TKA.