Treatment Trials

10 Clinical Trials for Various Conditions

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RECRUITING
Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty)
Description

The main objective of the study is to evaluate the safety, performance and clinical benefits of the Persona implant and its instrumentation in primary total knee arthroplasty

RECRUITING
Cemented vs Cementless Persona Keel RCT
Description

The main objective of this study is to evaluate the safety, performance, and clinical benefits of the Persona Keel cementless and cemented knee.

WITHDRAWN
A Randomized Controlled Trial for Partial Knee Arthroplasty
Description

This is a prospective, multi-center, two-arm, randomized, controlled post-market study to evaluate and compare the clinical accuracy of component placement in robotic-assisted UKA and that of traditional methods.

ACTIVE_NOT_RECRUITING
Persona Ti-Nidium Post-Market Clinical Follow-up
Description

The main objectives of this study are to evaluate overall clinical performance and safety of the Persona Ti-Nidium implant in total knee arthroplasty.

COMPLETED
The 3DKnee™ System: A Post-Market Study
Description

The purpose of this study is to evaluate the survivorship and efficacy of the Encore 3DKnee™ system in a group of patients who will receive the 3DKnee™ as a primary (first) orthopedic implant in the knee. Each knee will be designated as a separate subject and followed for a period of 2 years.

COMPLETED
Persona TM Tibia Clinical Outcomes Study
Description

The primary objective of this study is to evaluate clinical performance for the commercially available Persona TM Tibia used in primary cementless tibia total knee arthroplasty.

COMPLETED
NexGen TM Tibia Clinical Outcomes Study
Description

The objective of this study is to evaluate clinical performance for the commercially available NexGen TM Monoblock Tibia and NexGen TM Modular Tibia used in primary cementless tibia total knee arthroplasty.

COMPLETED
ROSA Robot Used in Total Knee Replacement Post Market Study
Description

This is a prospective, multicenter clinical study designed to facilitate the collection and evaluation of workflow efficiency, patient pain and function, and adverse event data. This clinical study will include Persona, NexGen, and Vanguard product families using the ROSA Total Knee Robotic System or conventional instrumentation. The primary objective of this study is to collect and compare clinical and surgical data using the commercially available ROSA Total Knee robotic instrumentation and conventional instrumentation.

ACTIVE_NOT_RECRUITING
Persona Total Knee Arthroplasty Outcomes Study
Description

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for commercially available Persona fixed bearing knee implants used in total knee arthroplasty. The assessment will include implant survivorship and clinical performance.

COMPLETED
Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee
Description

The purpose of the study is to assess the long-term performance of the NexGen LPS-Flex Mobile Bearing Knee in the treatment of patients with severe knee pain or degenerative knee disease.