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Osteoarthritis, Knee clinical trials

View clinical trials related to Osteoarthritis, Knee.

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NCT ID: NCT01832272 Recruiting - Clinical trials for Osteoarthritis, Knee

Reinflation After Early Tourniquet Release in Total Knee Arthroplasty

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

This study is aimed to determine the efficacy and the safety of the tourniquet reinflation after early tourniquet release in total knee arthroplasty, compared to the method of early deflation without reinflation. The investigators hypothesized that the reinflation after early release of the tourniquet would be effective in terms of improved visualization of the surgical field and decreased operation time and blood loss, whereas it would increase tourniquet-related complication due to longer tourniquet-use time.

NCT ID: NCT01832155 Completed - Quality of Life Clinical Trials

Yoga for Managing Knee Osteoarthritis in Older Women: a Feasibility Study

Start date: January 2011
Phase: N/A
Study type: Interventional

The study hypothesized that it is feasible and safe to use Hatha yoga in older women with knee osteoarthritis (OA), and practicing Hatha yoga regularly will help reduce pain and stiffness, enhance physical function, and improve quality of sleep and quality of life in older women with knee OA.

NCT ID: NCT01820676 Terminated - Knee Osteoarthritis Clinical Trials

iUni G2+ Prospective Study

Start date: July 15, 2013
Phase:
Study type: Observational

This study is designed to monitor long term clinical outcomes of the iUni G2+ unicompartmental knee replacement

NCT ID: NCT01820650 Terminated - Clinical trials for Osteoarthritis of the Knee

A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement System

Start date: February 2013
Phase:
Study type: Observational

This study is designed to observe the long term clinical outcomes of patient-specific knee arthroplasty in patients with osteoarthritis.

NCT ID: NCT01816282 Completed - Clinical trials for Osteoarthritis of the Knee

The Use of Fibrin Sealant to Reduce Bleeding After Total Knee Replacement

Start date: March 2011
Phase: N/A
Study type: Interventional

A randomized controlled study is performed to address the question of whether the topical application of a novel fibrin sealant, Evicel (Johnson & Johnson Wound Management, Ethicon, Somerville, NJ) in patient undergoing total knee replacement (TKR) reduce the perioperative blood loss and the need for allogenic blood transfusion compared to a control group. We hypothesize that fibrin sealant decrease the drop in post-operative hemoglobin level after total knee replacement.

NCT ID: NCT01811888 Recruiting - Knee Osteoarthritis Clinical Trials

Painful Knee Prosthesis. Relationship Between Endogenous Analgesia and Persistent Post Surgical Pain.

Start date: January 2013
Phase: N/A
Study type: Observational

This is a prospective, observational study, aimed to establish the relationship between an inefficient endogenous pain modulation before surgery (total knee arthroplasty; TKA) and the probability to develop chronic pain after surgery (persistent post surgical pain). Endogenous analgesia efficiency will be measured during the month previous to surgery using quantitative sensory testing (QST). Persistent post surgical pain will be defined as presence of pain in movement greater than 3 points in a 0-10 numerical scale in the operated knee, 6 months after surgery.

NCT ID: NCT01811563 Completed - Knee Osteoarthritis Clinical Trials

Total Knee Arthroplasty: Functional and Clinical Outcomes

Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the differences in functional and patient reported outcomes between total knee replacement (TKA) implants. In addition, this work will examine the correlation between functional assessments and patient reported outcomes following surgery. All subjects will complete assessments preoperatively, 4-6 weeks following TKA and then one year following TKA. Subjects will complete a series of patient reported outcomes as well as a series of functional outcomes at each of the time points of interest. The analysis will include a repeated measures design to determine differences between groups across time as well as correlations between the functional and patient reported outcomes. This work will hopefully determine the importance of using objective functional outcomes following TKA as well as determining the need for patient assessments out to one year following surgery.

NCT ID: NCT01810848 Terminated - Knee Osteoarthritis Clinical Trials

Pilot Study of Therapy With Hylan G-F 20 Exercise Capacity

CORT
Start date: June 2014
Phase: Phase 1
Study type: Interventional

Osteoarthritis of the knee is a degenerative joint disease that involves degradation of the joint. Symptoms include joint tenderness, pain, stiffness, locking, and occasionally an effusion. Over 40 million Americans also have cardiovascular disease in addition to their OA. Initiation and maintenance of even low-levels of physical activity is critical for management of cardiac risk. Patients with osteoarthritis have been shown to have poorer aerobic conditioning, lower daily physical activity levels and lower self-efficacy for exercise than non-OA cohorts. It has been established that there exists a consistent gradient across activity groups indicating greater longevity and reduced risk of CHD, CVD, and stroke, in more active individuals. Available research suggests the greatest gains in cardiovascular fitness occur in moving a sedentary individual to even low levels of physical activity, and 12 weeks is enough to demonstrate change in the risk profile of at-risk individuals. Finally, appropriate levels of aerobic and strength training have been shown to be beneficial in treatment of osteoarthritis of the knee. This study will evaluate the effectiveness of hylan G-F 20 (single injection preparation) in promoting greater levels of physical activity and fitness as measured by MET level compared to an exercise-only cohort; evaluating both the change in physical function as well as the cardiovascular risk profile. This is a randomized, single-blinded clinical trial comparing injection of the knee joint with Hylan GF-20 to sham procedure. Subjects will undergo a regular exercise program for 6 months following randomization.

NCT ID: NCT01809769 Completed - Knee Osteoarthritis Clinical Trials

Autologous Adipose Tissue Derived Mesenchymal Stem Cells Therapy for Patients With Knee Osteoarthritis

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

Two injections in total and 3 ml autologous adipose-tissue-derived stem cells(haMSCs) for each injection; time-points for intervention: 1) initial injection; 2) 3 weeks following initial injection.

NCT ID: NCT01806207 Completed - Clinical trials for Unilateral Knee Osteoarthritis

Durolane Compared to Saline in Patients With Unilateral Knee Osteoarthritis

Start date: February 2003
Phase: Phase 4
Study type: Interventional

This was a study that compared Durolane injections to saline injections in the treatment of unilateral osteoarthritis of the knee. The patients were randomly assigned one of the two treatments unaware of which treatment they received. The study was conducted at 13 centers in Germany, the United Kingdom and Sweden. Patients were followed for six weeks after study treatment.