Clinical Trials Logo
  1. Home
  2. Degenerative Joint Disease
  3. NCT03056534

R3 Delta Ceramic Acetabular System PAS U.S. — R3-PAS  

Degenerative Joint Disease Clinical Trial

Official title:
Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - US

Clinical Trial Summary

R3 Delta Post-Approval Study U.S.

Clinical Trial Description

Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - US The R3 Ceramic Acetabular System is indicated for use in skeletally mature patients requiring primary total hip arthroplasty due to non-inflammatory arthritis (degenerative joint disease) such as osteoarthritis, avascular necrosis, or traumatic arthritis. The expected timeline for the study is a total of approximately 5 years: 6 months for site initiation, 12 months for subject enrollment, 3 years until the last subject enrolled has reached the 3 year follow-up interval. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03056534
Study type Observational
Source Smith & Nephew, Inc.
Contact
Status Completed
Phase
Start date January 17, 2018
Completion date May 31, 2023
View Details
See also
  Status Clinical Trial Phase
Active, not recruiting NCT02380092 - Post Market Clinical Follow Up of LEGION™ Primary TKS With VERILAST™
Terminated NCT02900781 - Comparative Effectiveness of an Activity-specific Monitoring Device- StepRite N/A
Withdrawn NCT01920373 - Platelet-Rich Plasma vs Corticosteroid Injection as Treatment for Degenerative Pathology of the Temporomandibular Joint Phase 1
Completed NCT01510457 - Milnacipran for Chronic Pain in Knee Osteoarthritis Phase 4
Completed NCT01010763 - A Study on M2a Magnum Total Hip Arthroplasty N/A
Not yet recruiting NCT05229458 - Post Marketing Clinical Follow up Study to Evaluate the Performance and Safety of HYALEXO
Terminated NCT02904993 - Study Comparing Regional Anesthetic Blocks and Periarticular Infiltration for the Management of Post-operative Pain After Direct Anterior Total Hip Arthroplasty N/A
Completed NCT04399928 - EU Safety and Efficacy Study Regarding the R3 Acetabular Hip System
Completed NCT01305356 - Augment® Injectable Bone Graft Compared to Autologous Bone Graft as a Bone Regeneration Device in Hindfoot Fusions N/A
Recruiting NCT03090672 - Cellular & Biocellular Regenerative Therapy in Musculoskeletal Pain, Dysfunction,Degenerative or Inflammatory Disease N/A
Not yet recruiting NCT04918680 - Prospective Post-market Study Examining the Effectiveness of the EcoFit®
Terminated NCT01081886 - PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacement. N/A
Completed NCT01540851 - Adding Value in Knee Arthroplasty Post-total Knee Replacement (TKR) Care Navigator Trial N/A
Withdrawn NCT03488147 - Whether Proton Pump Inhibitors, Administered Prior to or After Surgery, Can Reduce the Incidence and/or Severity of Difficulty Swallowing Foods and/or Liquids,Following Anterior Cervical Surgery Phase 2
Completed NCT01379118 - Comparison of Clinical Outcomes and Performance of Total Knee Replacement Patients Before and After Surgery N/A
Completed NCT01391182 - Epsilon Aminocaproic Acid (EACA) for the Reduction of Blood Loss in Total Hip Arthroplasty (THA) N/A
Active, not recruiting NCT02543437 - Large Head X3 Study N/A
Recruiting NCT05357378 - Safety and Effectiveness of the HIT Reverse HRS N/A
Completed NCT01970631 - The Study of Physical Activity Rewards After Knee Surgery N/A
Recruiting NCT02686528 - Postoperative Hip Precautions After Total Hip Arthroplasty Via the Posterior Approach: A Prospective Randomized Trial N/A