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Total Knee Replacement clinical trials

View clinical trials related to Total Knee Replacement.

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NCT ID: NCT01463930 Completed - Clinical trials for Total Knee Replacement

Audiovisual Videodisc Education and Modification of Expectations With Total Knee Replacement (TKR)

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

Information provided to patients modifies their expectations with surgery. The effects of preoperative audiovisual information on expectations with total knee replacement (TKR) have not been investigated. The purposes of this study were to investigate the effectiveness of an educational videodisc on the modification of pre-operative patients' expectations with TKR and to find a biophysical profile of subjects in whom this videodisc could be most effective. It was hypothesized that patients receiving standard information plus additional medical information through audiovisual videodiscs would modify their pre-operative expectations more than those only receiving the standard information through medical interviews.

NCT ID: NCT01340144 Completed - Clinical trials for Total Knee Replacement

Evaluation of Patellar Crepitus Following Total Knee Arthroplasty

Start date: April 2011
Phase: N/A
Study type: Observational

Analyze clinical data for a group of subjects implanted with a new surgical device designed to reduce the incidence of patellar crepitus following PCL-substituting TKA and compare that to a control group of subjects implanted with a TKA design known to have an incidence of patellar crepitus of approximately 5%.

NCT ID: NCT01307202 Completed - Post Operative Pain Clinical Trials

Morphine Consumption in Joint Replacement Patients, With or Without Gabapentin Treatment

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

Total knee arthroplasty is amongst the most painful procedures postoperatively, and pain management can be a challenge. Different measures have been introduced to manage severe postoperative pain int hese patients. Previous studies have investigated gabapentin in acute postoperative pain and demonstrated reducted pain, postoperative morphine consumption, morphine related side effects, and postoperative pain scores. To date, this analgesia adjunct has yet to be investigated in total joint arthroplasty patients.

NCT ID: NCT01274546 Completed - Clinical trials for Total Knee Replacement

Long Term Foundation Knee Study

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

The purpose of this study is to obtain long-term (10+ yrs) clinical and patient outcomes data on patients who received the cruciate-retaining Foundation Knee system during or prior to the year 2000.

NCT ID: NCT01189565 Completed - Clinical trials for Total Knee Replacement

Continuous Postoperative Pulse Oximetry in Patients Presenting for Total Hip and Total Knee Replacement

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

The purpose of this study is to evaluate the incidence of low levels of oxygen as determined by standard pulse oximetry monitor in patients who have had total hip or knee replacement/revision.

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: 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: 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: NCT00493792 Completed - Clinical trials for Arthroplasty, Replacement, Knee

X-3 Polyethylene Survival Outcomes Study

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

A prospective, randomized, blinded clinical trial is proposed to compare Stryker Orthopaedics N2Vac Polyethylene to their X3 Polyethylene when used with the Triathlon Posterior Stabilized (PS) total knee system.