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Knee Replacement Arthroplasty clinical trials

View clinical trials related to Knee Replacement Arthroplasty.

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NCT ID: NCT06201195 Completed - Nerve Block Clinical Trials

Anterior Cutaneus Nerve and Distal Adductor Canal Block With USG for Total Knee Replacement Analgesia

Start date: October 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare analhesia effects of adductor canal blockade versus distal adductur canal blockade added anterior cutaneus nerve block in total knee arthroplasty. The main questions it aims to answer are: - question 1: does distal adductor canal blockade + anterior cutaneus nerve blokade superior analgesia then adductor canal block for undergoing TKP? - question 2: does distal adductor canal blockade + anterior cutaneus nerve blokade decrease drain place pain on anterolateral face of knee?

NCT ID: NCT03954379 Completed - Clinical trials for Knee Replacement Arthroplasty

IPACK Study in Total Knee Arthroplasty Patients

Start date: October 24, 2019
Phase: Phase 4
Study type: Interventional

This study proposes to compare current multimodal analgesic treatment for TKA with a new multimodal analgesic regimen to demonstrate decreased opioid requirement, time to rehabilitation, and time to reach hospital discharge.

NCT ID: NCT02294890 Not yet recruiting - Fibrosis Clinical Trials

Knee Stiffness in Fibrosis Diathesis

Start date: January 2015
Phase: N/A
Study type: Observational

At the standard follow-up moment one year after primary TKA for gonarthrosis, all patients will be checked for signs of fibrosis diathesis. This will be done by examining their hands for Dupuytren's nodules and contractures and recording risk factors associated with increased severity and risk of recurrence of Dupuytren's contracture. These include family history, bilateral DD, and ectopic lesions, age of onset less than 50 years, male gender, Ledderhose disease, first ray involvement, multiple ray involvement and ectopic fibromatosis. This way, two groups of patients will be identified: those with and those without signs of fibrosis diathesis. For both groups, the range of motion (ROM) of the operated knee at 3 and 6 months will be retrieved in the charts, the ROM at 12 months will be measured at that time. Also, additional procedures performed to increase ROM postoperatively will be retrieved from the charts (e.g. continuous passive motion, mobilization under anesthesia). Other causes for knee stiffness will have to be recorded, since these will be the most important exclusion criteria. In the patients with clear signs of finger contractures, any impression of increase of contracture over the past 12 months will be recorded.

NCT ID: NCT02242591 Completed - Clinical trials for Knee Replacement Arthroplasty

Effect of Adductor Canal Block vs. Placebo on Muscle Strength, Mobilisation and Pain After Total Knee Arthroplasty

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

The purpose of this study is to evaluate the effect of adductor canal block (ACB) vs. placebo on muscle strength, mobility and pain on the first postoperative day after total knee alloplastic (TKA).

NCT ID: NCT01714492 Completed - Knee Prosthesis Clinical Trials

Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA

Sigma MB TKA
Start date: April 2012
Phase:
Study type: Observational

Utilize previously developed mathematical model to determine in vivo knee mechanics (kinematics, forces, stresses, areas and sound) for subjects having a Sigma Posterior Stabilizing (PS) mobile bearing (MB) total knee arthroplasty (TKA). There are several hypotheses for this study, although the most prominent is: Subjects having a Sigma RP PS TKA will experience polyethylene bearing rotation at 10 years post-operative, similar to their previous evaluations at six months, two years and five years.

NCT ID: NCT01163214 Completed - Postoperative Pain Clinical Trials

Management of Postoperative Pain After Total Knee Replacement.

Start date: July 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare two methods of postoperative pain management in patients undergoing total knee replacement.