Clinical Trials Logo

Osteoarthritis, Knee clinical trials

View clinical trials related to Osteoarthritis, Knee.

Filter by:

NCT ID: NCT02104726 Withdrawn - Osteoarthritis Clinical Trials

"Blind" vs. Fluoroscopy-Guided Steroid Injections for Knee Osteoarthritis

Start date: July 2014
Phase: N/A
Study type: Interventional

To compare relative efficacy of intraarticular steroid injection using anatomic landmarks vs. fluoroscopy guided technique in decreasing knee osteoarthritis pain 1 month after the procedure.

NCT ID: NCT02003131 Withdrawn - Clinical trials for Osteoarthritis of the Knee

Safety and Feasibility Study of Mesenchymal Trophic Factor (MTF) for Treatment of Osteoarthritis

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Allogeneic mesenchymal trophic factors (MTF) from human umbilical cord tissue-derived mesenchymal stem cells (UC-MSC) injected into the knee joints of 20 patients (group 1) or injected subcutaneously into 20 patients (group 2) is a safe and useful procedure for inducing joint function improvements in osteoarthritis (OA) patients with grade 2, 3, or 4 radiographic OA severity.

NCT ID: NCT01938274 Withdrawn - Knee Osteoarthritis Clinical Trials

Leisure Expectations About Physical Activity Study

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

To pilot test an activity-focused intervention that educates patients undergoing total hip (THA) or total knee (TKA) arthroplasty due to osteoarthritis about the appropriate type, frequency, intensity, and duration of expected leisure activities after surgery and to determine if the intervention changed expectations.

NCT ID: NCT01923909 Withdrawn - Osteoarthritis Clinical Trials

Intraarticular Platelet-rich Plasma Injections Versus Corticosteroid Injections in Primary Knee Osteoarthritis

Start date: April 2013
Phase: Phase 4
Study type: Interventional

Aim: To study and compare the clinical effects of platelet-rich plasma (PRP) injections and intra-articular (IA) corticosteroid injections in patients with primary osteoarthritis (OA) of the knee. This study aims to demonstrate this by using the Oxford Knee Score and Western Ontario and McMaster Universities Arthritis Index (WOMAC) to illustrate quantifiable difference between the two treatment modalities. Patient satisfaction will be compared by utilizing the Short-Form Survey-12 (SF-12) Score. Our null hypothesis states that intra-articular PRP injections is more beneficial in the long-term treatment of primary OA of the knee.

NCT ID: NCT01890902 Withdrawn - Clinical trials for Acute Pain (Flare) Associated With Osteoarthritis (OA) of the Knee

Efficacy and Safety of Impracor (Ketoprofen 10% Cream) Compared With Placebo in the Treatment of Acute Pain (Flare) Associated With Osteoarthritis of the Knee

Start date: August 2013
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to assess analgesic efficacy of Impracor (Ketoprofen 10% Cream) compared to placebo for acute pain associated with OA flare of the knee.

NCT ID: NCT01614288 Withdrawn - Clinical trials for Medial Compartment Osteoarthritis of the Knee

High Tibial Osteotomy (HTO) With or Without Arthroscopy of the Knee Joint

Start date: n/a
Phase: N/A
Study type: Interventional

Participants will be randomized to undergo a High Tibial Osteotomy (HTO) with or without a knee scope. Patients will be tested in the Gait Lab, will fill out quality-of-life questionnaires, and have a clinical evaluation done preoperative and at each follow-up visit.

NCT ID: NCT01565070 Withdrawn - Knee Osteoarthritis Clinical Trials

Osteoarthritis in Older Adults: Recovery of Mobility and Pain With a Topical Analgesic

Start date: April 2012
Phase: Phase 3
Study type: Interventional

Biofreeze® is a topical ointment that has menthol and alcamphor. Its analgesic effect lies in the stimulation of A and C fibers by cold and nociceptive stimulation, respectively, which is produced by menthol, apparently through the newly discovered receptor TRPM8 (Transient Receptor Potential melastatin-8) The aim of this study is to investigate if BIOFREEZE ® treatment (Performance Health Inc., Export, PA) improves symptoms associated with moderate knee osteoarthritis, which would decrease the immobility and isolation in older adults.

NCT ID: NCT01488175 Withdrawn - Clinical trials for Osteoarthritis of the Knee

Clinical and Stereoradiological Comparison of the Results After Primary Cemented Total Knee Arthroplasty Inserted With or Without the Use of a Tourniquet

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

The purpose of this study is to investigate if the use of a tourniquet during insertion of a cemented primary total knee arthroplasty will influence clinical and radiological (measured with RSA X-ray technique) outcome.

NCT ID: NCT01469507 Withdrawn - Knee Osteoarthritis Clinical Trials

Efficacy and Safety Study in Patients Suffering From Knee Osteoarthritis

VESTA
Start date: n/a
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare a combination of hyaluronic acid and chondroitin sulfate (V0220) to Hyalgan® on pain relief in patients with symptomatic knee osteoarthritis (OA) over 24 weeks when administered in three weekly injections. Chondroitin sulfate is one of the components of cartilage. Studies have shown that chondroitin sulphate improves the quality of the hyaluronic acid produced in the joint. The benefit of V0220 combination is based on two main physicochemical properties, in line with the characteristics of osteoarthritic disease: optimising the rheological behaviour and improving the buffering effect on synovial flow ("outflow buffering").

NCT ID: NCT01438918 Withdrawn - Knee Osteoarthritis Clinical Trials

X-Ray Study Investigating The Safety And Efficacy Of SD-6010 In Subjects With Osteoarthritis Of The Knee

Start date: March 2012
Phase: Phase 3
Study type: Interventional

The objective of this 2-year study is to evaluate the safety, tolerability and disease modifying efficacy of SD 6010, an inhibitor of inducible nitric oxide synthase (iNOS). The efficacy of SD-6010 will be evaluated by radiography using joint space narrowing in the medial tibiofemoral compartment of the study knee as the primary endpoint.