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Osteo Arthritis Knee clinical trials

View clinical trials related to Osteo Arthritis Knee.

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NCT ID: NCT04730271 Active, not recruiting - Osteoarthritis Clinical Trials

Comparison of Alignment Achieved Using the VELYS Robotic-Assisted Solution Versus Manual Instrumentation in Total Knee Arthroplasty

Start date: February 9, 2021
Phase: N/A
Study type: Interventional

The purpose of this post-market research study is to gather clinical and radiographic (X-ray) information about total knee replacement surgeries completed with the VELYS Robotic-Assisted Solution and with standard manual instrumentation. The VELYS Robotic-Assisted Solution helps the surgeon to plan bone cuts and then accurately achieve the planned cuts during the total knee replacement surgery. The study aims to compare how well the VELYS Robotic-Assisted system enables the surgeon to position the implants exactly as planned compared to manual instrumentation.

NCT ID: NCT04525950 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Robotized Navigation Compared to Conventional Technique in Total Knee Replacement

NavioRCT
Start date: September 7, 2020
Phase: N/A
Study type: Interventional

Navio is a new generation of computer navigation systems allowing intraoperative navigation of the bone cuts relative to both ligaments and skeletal axes, prior to bone removal. An improved accuracy is incorporated by the use of robotics in a burr for bone removal. This study investigates whether this advanced technology leads to better clinical or radiostereometric results, by comparing one group operated with Navio to another group operated with conventional technique.

NCT ID: NCT03865550 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Post-op Ketamine Study

Start date: March 28, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to establish the effect of sub-anesthetic dosing of ketamine with spinal anesthesia during total knee arthroplasty on post-operative pain and narcotic consumption. We hypothesize that sub-anesthetic ketamine will decrease post-operative pain and narcotic consumption and may secondarily lead to shorter lengths of stay, faster rehabilitation, improved postoperative outcomes and patient satisfaction.

NCT ID: NCT03631030 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Cooled RF Lesion MRI Characteristics

Start date: February 25, 2018
Phase: N/A
Study type: Interventional

This Prospective, Single-center, Pilot Study will assist in gaining an understanding of the actual CRFA lesions in an in vivo situation in areas where CRFA is utilized as a standard of care treatment option for the relief of chronic pain (cervical facet joints, thoracic facet joints, lumbar facet joints, Sacroiliac (SI) region, hip and knee).

NCT ID: NCT03563131 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Tibial and Femoral Components Migration and Adaptive Bone Remodeling After Insertion of Persona® TKA

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this study: In a prospective randomized study with 2 years of follow-up we want to compare the migration of the uncemented trabecular metal (TM) versus the cemented tibial and femoral components of the new Persona® total knee arthroplasty (TKA) assessed by model based radiostereometric analysis (MB-RSA). Also, we want to compare the adaptive bone remodeling induced by the uncemented TM versus the cemented tibial and femoral components of the new Persona® TKA assessed by dual energy-X-ray (DEXA). Data generated for both above mentioned, will be also compared with historical RSA and DEXA data for the NexGen TKA using TM tibia modular and monoblock.

NCT ID: NCT03385759 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Trial of Unicompartmental Versus Total Knee Arthroplasty

Start date: May 22, 2018
Phase: N/A
Study type: Interventional

This study is a prospective, randomized trial to compare patient outcomes of unicompartmental knee arthroplasty (UKA) and total knee arthroplasty (TKA) for the treatment of medial compartment osteoarthritis.

NCT ID: NCT03060057 Active, not recruiting - Clinical trials for Osteo Arthritis Knee

Prospective Post Approval Clinical Follow-Up Study of the Commercially Available U2 Knee™ System - "U-Propel Study"

U-Propel
Start date: March 30, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate both short and long term clinical performance and safety of the commercially available U2 Knee™ System.