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Total Knee Replacement clinical trials

View clinical trials related to Total Knee Replacement.

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NCT ID: NCT02873637 Completed - Clinical trials for Total Knee Replacement

Adductor Under Sartorial Canal Catheter (KTT) Versus Femoral Catheter (KTF) in a Quick Rehabilitation Process After Total Knee Replacement

KTSS
Start date: January 2017
Phase: N/A
Study type: Interventional

The main objective of this study is to show that postoperative Total Knee Replacement (TKR), an analgesic perineural catheter in position under sartorial (KTSS) best preserves motor quadriceps femoral perineural catheter that (KTF) infused with even low doses of local anesthetics, this motor being evaluated by a semi quantitative simple clinical test locking of the knee feasible at the bedside. Patients will be randomized in two arms: - catheter in position under sartorial (experimental group) - femoral catheter (control group)

NCT ID: NCT02707419 Completed - Clinical trials for Total Knee Replacement

Action Observation in Knee Replacement

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

Postoperative rehabilitation is required for a successful outcome following total knee arthroplasty. Traditionally rehabilitative programs aim to increase range of motion, to strengthen quadriceps, to restore normal gait, and to recover independence in activities of daily living. In the last decade action observation treatment, in addition to conventional physiotherapy has been proposed as a treatment method in rehabilitative medicine. There is growing evidence of the applicability of action observation training in rehabilitative medicine, indeed it has been applied in the rehabilitation of stroke of Parkinson disease of cerebral palsy and of aphasia. Nevertheless those are small studies and one of them included a mixed population of hip and knee arthroplasty.

NCT ID: NCT02706990 Completed - Clinical trials for Total Knee Replacement

Fluoroscopic Analysis of Total Knee Replacement With a Kinematic Retaining or a Posterior Stabilized Design

Start date: January 2016
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the in vivo kinematics of TKA performed with two different prosthesis: a kinematic retaining (Physica KR) and a posterior-stabilized (Physica PS) design by means of fluoroscopic analysis during activities of daily living (rising from a chair, stairs climbing, leg extension). In comparison with asymptomatic knee. Patterns of femoral rollback will be analyzed to assess if they are motor-task dependent and correlated with clinical outcomes.

NCT ID: NCT02670499 Completed - Clinical trials for Total Knee Replacement

Study Comparing GAP-Flex to CPM Therapy in Treatment of TKR

GAP-Flex
Start date: November 18, 2015
Phase: N/A
Study type: Interventional

Post Market TKR study

NCT ID: NCT02655809 Completed - Clinical trials for Total Knee Replacement

Physica KR Fluoroscopy Study

Start date: June 2015
Phase: N/A
Study type: Interventional

The aim of this study is to assess the in vivo kinematics and range of motion of a single-surgeon clinical series of TKA performed with a fixed-bearing cruciate retaining total knee arthroplasty that has a roll-back mechanism and compare it with the kinematic of the normal healthy knee. Patients would be evaluated by fluoroscopic examination during weight bearing activities (lounging, kneeling and stairs climbing).

NCT ID: NCT02468934 Completed - Pain Clinical Trials

Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System

Start date: October 22, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if electrical stimulation (small levels of electricity) can safely and effectively reduce pain following total knee replacement (or total knee arthroplasty (TKA)). This study involves a device called the SPRINT System. The SPRINT System delivers mild electrical stimulation to nerves in the leg that received the knee replacement. The SPRINT System includes a small wire (called a "lead") that is placed through the skin in the upper leg. It also includes a device worn on the body that delivers stimulation (called the SPRINT Stimulator).

NCT ID: NCT02413996 Completed - Osteoarthritis Clinical Trials

Effects of Virtual Reality Rehabilitation in Patients With Total Knee Arthroplasty

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

The aim of this study is to assess the efficacy of virtual rehabilitation through the Virtual Reality Rehabilitation System (VRRS) versus traditional rehabilitation improving the functional outcomes after primary Total Knee Arthroplasty (TKA).

NCT ID: NCT02143232 Completed - Clinical trials for Total Knee Replacement

Post Op Home Monitoring After Joint Replacements

POHM
Start date: April 2014
Phase: N/A
Study type: Interventional

The investigators propose to deploy an interactive device to monitor the patient's recovery and vital signs at home after joint replacements. These will be early discharge patients on the same day or the next morning. The goal will be to support early discharges by creating a safe, controlled, and monitored environment at home.

NCT ID: NCT02125903 Completed - Clinical trials for Total Knee Arthroplasty

Comparison of Continuous Femoral Nerve Block and Adductor Canal Block After Total Knee Replacement Therapy

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

The blockade of the femoral nerve (FNB) is the most common postoperative pain therapy after total knee replacement. Because of motor-driven weakness of the quadriceps muscle induced by femoral nerve block mobilization of Patients is difficult even dangerous (falls) and hospital stays are extended. An alternative method could be an adductor canal block (ACB). Anatomical studies of the adductor canal demonstrated that the adductor canal contains the saphenous nerve, a pure sensory nerve for medial and anterior aspects of the knee and the tibia without any motor function. This prospective, double-blinded, randomized study investigates the effect of FNB and ACB on quadriceps motor weakness and analgesia determined by Numeric Rating Scale (NRS). We expect the ACB to be superior in muscle strength but equal in pain score. Both groups receive an additional anterior sciatic nerve block for complete sensory block of the operated knee

NCT ID: NCT02067533 Completed - Clinical trials for Total Knee Replacement

Flexion Versus Extension Soft Tissue Repair in Total Knee Arthroplasty

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

The purpose of the present study is to determine the influence of position of soft tissue repair (flexion versus extension) in post operative range of motion(ROM) and functional outcome in patients who underwent primary total knee arthroplasty (TKA).