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Arthropathy of Knee clinical trials

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NCT ID: NCT02619409 Completed - Arthropathy of Knee Clinical Trials

Evaluation of the Duration of Bupivacaine Spinal Block in Orthopedic Procedures With and Without Epinephrine Wash

Start date: February 11, 2016
Phase: N/A
Study type: Interventional

Bupivacaine spinal is commonly performed as the primary anesthetic for orthopedic procedures. In some cases the duration of the block is inadequate. An epinephrine wash is sometimes performed to prolong the duration of the block. The epinephrine wash may prolong the duration of the block, and if it does, to what extent?

NCT ID: NCT02584725 Completed - Arthropathy of Knee Clinical Trials

Tranexamic Acid Dosing for Total Joint Arthroplasty

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of increasing doses of tranexamic acid (TXA) on limiting blood loss during total knee and total hip arthroplasty as defined by a change in hemoglobin from pre-operative baseline to the first post-operative day.

NCT ID: NCT02330185 Completed - Arthropathy of Knee Clinical Trials

Comparison of Two Anatomic Landmarks With Ultrasonography in Spinal Anesthesia

Start date: January 2015
Phase: Phase 4
Study type: Interventional

The most used anatomical landmark for application of spinal anesthesia is Tuffier's line. Other alternative landmark is tenth rib. However there is no trial that compare these landmarks based on using ultrasonography.

NCT ID: NCT01676038 Completed - Arthropathy of Knee Clinical Trials

Pinless-Navigated Versus Conventional Total Knee Arthroplasty

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

The success of total knee arthroplasty depends on a number of factors including pre-operative range of movement, obesity, medical comorbidities, prosthesis design, preparation and implantation of the prosthesis, soft tissue balancing, as well as implants alignment. Optimal placement of the implants within 3° of the mechanical axis of the lower limb has been proven to reduce wear and early implant failure. Compared to conventional techniques, computer-Aided Navigation total knee arthroplasty has been widely used in the last decade and have been proven to improve the accuracy of prosthesis placement and lower limb alignment by reducing the number of outliers with more than 3° deviation from the mechanical axis. However, its use also involves a steep learning curve, high initial capital cost and longer duration of surgery. Traditional computer-navigated TKA using optical tracking systems also requires fixation of the femoral and tibial reference arrays to bone using anchoring pins. Complications reported with the use of these pins include either femoral or tibial fracture, pin site pain, pin site infection and osteomyelitis. The investigators study aims to investigate the accuracy of a new pinless navigation system for TKA that will avoid these complications.

NCT ID: NCT01320371 Completed - Arthropathy of Knee Clinical Trials

Analysis of Standard Versus Barbed Sutures in Primary Total Knee Arthroplasty.

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

The purpose of this prospective study is determine if barbed sutures are more efficient, have comparable complication rates, clinical outcomes, and cosmesis outcomes versus traditional knotted sutures when used in the closure of primary total knee arthroplasty (TKA). Barbed suture has been associated with improved closure efficiency and safety in TKA in prior studies. The investigators performed a multicenter randomized controlled trial to determine the efficiency and safety of this technology in TKA. The investigators prospectively randomized 411 patients undergoing primary TKA to either barbed running (n=191) or knotted interrupted suture closure (n=203). Closure time was measured intraoperatively. Cost analysis was based on suture and operating room time costs.

NCT ID: NCT01135160 Recruiting - Arthropathy of Knee Clinical Trials

Evaluation of Weight Bearing After Total Hip and Knee Replacement

Start date: November 2014
Phase:
Study type: Observational

The regime in the aftercare after total hip and knee arthroplasty(THA/TKA) differs a lot between orthopedic surgeons concerning weight bearing. The type of implant and the way of implants' anchoring are considered. In the literature there is no data so far about the way patient take care of the recommended weight bearing during the first 6 weeks after THA and TKA. Over a one year period starting August 2010 all patients undergoing TKA or THA at the investigators institution will have a technical device in their shoes (sole) to measure the load in each step they do in these shoes during the first 6 weeks. Patients are asked to fill out a standardised pain protocol every day (VAS) and document need of pain medication. The investigators recommend 20kg of weight on the operated leg for 6 weeks and full weight bearing at the end of week six. The investigators believe that patients will adjust weight bearing to their level of pain and not to their surgeons recommendations.

NCT ID: NCT00965146 Terminated - Arthropathy of Knee Clinical Trials

Scorpio® Cruciate Retaining (CR) Outcomes Study

Start date: June 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the design and functional performance of the Scorpio® Cruciate Retaining (CR) Total Knee System.

NCT ID: NCT00808613 Withdrawn - Arthropathy of Knee Clinical Trials

Optetrak Posterior Stabilized Versus Optetrak Hi-Flex

Start date: December 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs.