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Total Knee Replacement clinical trials

View clinical trials related to Total Knee Replacement.

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NCT ID: NCT01037400 Withdrawn - Clinical trials for Total Knee Replacement

Biochemical Approach to Measuring Surgical Trauma

Start date: February 2010
Phase: N/A
Study type: Observational

This study will examine the magnitude and time course of changes in circulating (serum and plasma) biomarker concentrations associated with musculoskeletal injury created by total knee replacement surgery. The sensitivity to injury will be characterized by the changes in mean serum concentration before and after surgery. Specificity for the injured state will be evaluated comparing the baseline to peak change (injury response) with the pre-surgery to follow-up baseline fluctuation (i.e. measurement noise).

NCT ID: NCT01030848 Unknown status - Osteoarthritis Clinical Trials

Time-dependent Improvement of Functional Outcome Following LCS Rotating Platform TKR

Start date: February 2003
Phase: N/A
Study type: Observational

The objective of this prospective study is to determine (1) the time course of patient-relevant functional outcome evaluated by the Knee injury and Osteoarthritis Outcome Score (KOOS) and (2) the time course of range of motion (ROM) the first four years following TKR using the LCS rotating platform prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest.

NCT ID: NCT00935155 Recruiting - Clinical trials for Total Knee Replacement

Effectiveness of Acupuncture as an Adjunct to Rehabilitation After Knee Arthroplasty

Start date: January 2009
Phase: N/A
Study type: Interventional

No randomized trials have tested the effectiveness of acupuncture as a supplement to rehabilitation after total knee replacement. Studies from related fields, however, have shown reduction of symptoms as a result of acupuncture treatment in patients with knee pain caused by severe osteoarthritis in the knee. Furthermore, studies have reported that the need of pain medication was lower when acupuncture treatment was performed immediately after knee surgery. The aim of this study is to test whether acupuncture can reduce pain and improve disability as a supplement to rehabilitation after total knee replacement. One hundred and seventy patients will be allocated by drawing lots to either a treatment group receiving exercise therapy and acupuncture or a group receiving exercise therapy alone. Treatment will start 3 weeks after surgery at the latest. Outcome of treatments will be measured at completion of treatment and at 3 months follow-up by pain- and disability questionnaires as well as the recording of walking capacity.

NCT ID: NCT00910013 Completed - Clinical trials for Total Knee Replacement

Femoral Block With or Without Ropivacaine for Analgesia After Total Knee Replacement (TKR)

TKR
Start date: April 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Total knee replacement is a painful procedure. Many solutions have been proposed to diminish the post-operative doses of narcotics, including nerve blocks. The purpose of the study is to compare if the adjunction of intra-articular ropivacaine to a femoral block is more effective on narcotics consumption than the block alone after TKR.

NCT ID: NCT00909064 Not yet recruiting - Clinical trials for Total Knee Replacement

The Effects of Arixtra on Wound Drainage Following Total Joint Arthroplasty

Start date: June 2009
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that Arixtra patients will be less likely to experience wound infection than patients who have received low-molecular weight heparin, coumadin or aspirin with mechanical compression.

NCT ID: NCT00878358 Completed - Osteoarthritis Clinical Trials

Hydrotherapy Versus Physiotherapy for Short-term Rehabilitation After Primary TKR

Start date: June 2009
Phase: N/A
Study type: Interventional

Primary objective: To compare the effects of short term therapy post total knee replacement (TKR) between a hydrotherapy treatment group and a physiotherapy treatment group. Secondary objectives: To compare the effects of short term therapy post total knee replacement (TKR) between a hydrotherapy treatment group and a physiotherapy treatment group based on measurements of timed up and go (TUG, as primary outcome), range of motion, pain and quality of life.

NCT ID: NCT00815958 Terminated - Clinical trials for Total Knee Replacement

Embolic Events Detected During Total Knee Arthroplasty With the Use of RIA (Reamer-Irrigator-Aspirator)

Start date: December 2007
Phase: N/A
Study type: Interventional

The embolisation of fat and bone marrow during long bone instrumentation is a well-known complication of major joint replacement surgery. Clinically significant venous thromboembolic disease, cardiopulmonary dysfunction,cerebral emboli, and death have all been described. Because the intravasation of medullary contents is caused by increased pressure during canal instrumentation, the use of the Synthes RIA (Reamer-Irrigator-Aspirator), a negative pressure-irrigated high-speed reamer, may result in a lower incidence of embolism. This controlled clinical trial will evaluate the utility of the RIA in reducing the frequency and severity of embolic events as detected by intraoperative transesophageal echocardiography (TEE) and transcranial Doppler (TCD) during total knee arthroplasty (TKA) surgery.

NCT ID: NCT00795223 Completed - Post Operative Pain Clinical Trials

Comparative Pain Control Between 0.2 or 0.3 Spinal Morphine and 0.25 or 0.5 % Bupivacaine for FNB After TKA

Start date: October 2008
Phase: Phase 4
Study type: Interventional

Comparative efficacy of 24 and 48 hours post operative pain control in single total knee replacement between intrathecal bupivacaine with 0.2 or 0.3 mg morphine together with 0.25 or 0.5 % bupivacaine for single femoral nerve block

NCT ID: NCT00755300 Completed - Clinical trials for Venous Thromboembolism

Total Knee Arthroplasty And Thromboembolism: A Comparison Between Two Surgical Techniques

Start date: June 2006
Phase: N/A
Study type: Observational

In patients undergoing total knee arthroplasty, thromboembolism is a common occurrence, especially following tourniquet deflation. The resulting cardiopulmonary emboli can potentially lead to hypoxemia, hypotension, hemodynamic collapse and post operative cognitive dysfunction due to emboli. The standard surgical technique involves placing an intramedullary rod in the femur to determine the angle and degree of resection from the end of the femur. A new surgical technique utilizes computer navigation system to perform the desired cuts in the appropriate position. The investigators hypothesize that the avoidance of intramedullary instrumentation in computer assisted total knee replacement will result in fewer thromboembolic events compared with the standard technique using manual instrumentation in the femur. The present study will test this hypothesis by quantifying the extent of thromboembolism during both surgical techniques.

NCT ID: NCT00512421 Terminated - Clinical trials for Total Knee Replacement

Navigated EM Total Knee Replacement: Accuracy Study

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

The use of computer-assisted surgery by orthopedic surgeons experienced in the performance of total knee arthroplasty may result in better overall limb and implant alignment and fewer outliers as compared with the findings after manual total knee arthroplasty. The alignment results in previous studies were based on radiographic measurements. The sensitivity of radiographic assessment of limb and implant alignment may not be significant enough to distinguish small differences between computer-assisted surgery and manual techniques. It is possible that alignment differences that were too minor to be exposed on standard radiographs might result in long-term differences in the durability of arthroplasties performed with use of computer-assisted surgery or manual techniques. Moreover it is possible to measure additional implant positioning parameters with computed tomography (CT) technology. In this study, the investigators would like to add new method, for accurate measurement of implant alignment and to correlate its results with clinical data.