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Chronic Osteoarthritis clinical trials

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NCT ID: NCT04338893 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

ROSA Total Knee Post Market Study EMEA

Start date: December 15, 2020
Phase: N/A
Study type: Interventional

This is a prospective, multicenter clinical study designed to facilitate the collection and evaluation of surgical workflow efficiency, patient pain and function outcome and adverse events data. This study might include Persona, Nexgen and Vanguard product families using the ROSA Total Knee Robotic system or conventional instrumentation. The primary objective is to evaluate the accuracy of implant alignment for ROSA Total Knee robotic instrumentation compared to conventional instrumentation.

NCT ID: NCT03970629 Terminated - Clinical trials for Rheumatoid Arthritis

ROSA Total Knee Investigational Testing Authorization Study

Start date: June 20, 2019
Phase: N/A
Study type: Interventional

This is a prospective, single-center 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 Total Knee components using the ROSA Total Knee Robotic System or conventional instrumentation.

NCT ID: NCT03969654 Completed - Clinical trials for Rheumatoid Arthritis

ROSA Robot Used in Total Knee Replacement Post Market Study

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT00902837 Completed - Clinical trials for Chronic Osteoarthritis

OXN PR Compared to OxyPR to Demonstrate Non-inferiority in Pain & Locomotor Function & Improvement in Symptoms of Constipation in OA Subjects

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The primary objectives are - to demonstrate that the treatment with OXN PR tablets is non-inferior to the treatment with OxyPR with regards to analgesic efficacy and locomotor function. - to demonstrate that subjects with moderate to severe OA pain taking oxycodone/naloxone prolonged release tablets have improvement in symptoms of constipation compared to subjects taking oxycodone prolonged release tablets alone