Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the clinical outcomes (range of motion, pain, function, radiographic stability, and health related quality of life) of patients receiving the Triathlon® Cruciate Retaining (CR) Total Knee System. These outcomes will be evaluated by comparing pre-operative to post-operative scores, as well as to a control group. The control group is the Scorpio® CR Total Knee System.

Clinical Trial Description

The Triathlon® Cruciate Retaining (CR) Total Knee System components are for use in cemented total knee arthroplasty for painful, disabling joint disease of the knee resulting from non-inflammatory degenerative joint disease (including osteoarthritis, traumatic arthritis or avascular necrosis) or rheumatoid arthritis (excluded from this study according to protocol). The components are designed to improve range of motion (ROM) and stability. This study serves to demonstrate that subjects have reduced pain, increased ROM and improved stability following implantation with the Triathlon Cruciate Retaining (CR) Total Knee System as compared to the historical control. ;

Study Design

Related Conditions & MeSH terms

Arthroplasty, Replacement, Knee

Clinical Trial Details

NCT number	NCT00957723
Study type	Interventional
Source	Stryker Orthopaedics
Contact
Status	Completed
Phase	N/A
Start date	February 2005
Completion date	September 26, 2017

View Details

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT05666479` - CGM Monitoring in T2DM Patients Undergoing Orthopaedic Replacement Surgery
Recruiting	`NCT05002387` - Diagnostic Knee Needle Arthroscopy in Predicting Unicompartmental Knee Osteoarthritis	N/A
Recruiting	`NCT06080763` - Biomechanics and Clinical Outcomes in Responders and Non-Responders
Completed	`NCT03008967` - A Study of Patients Undergoing Total Knee and Hip Arthroplasty at a Regional Hospital in Denmark	N/A
Withdrawn	`NCT02255877` - ZIPS Study - Zip Incision Approximation vs. STAPLE	Phase 4
Completed	`NCT02642731` - Kidney Biomarkers of Acute Kidney Injury in Patients With Knee Arthroplasty	N/A
Completed	`NCT01799772` - The Feasibility of a Comprehensive Behavioral Intervention in Patient Post TKA	Phase 1/Phase 2
Completed	`NCT02525588` - Polyethylene Wear Study on the Triathlon Total Knee Prosthesis	N/A
Completed	`NCT02520531` - Scorpio Posterior Stabilised (PS) vs Scorpio NRG ("Energize") PS - Total Knee Arthroplasty	N/A
Completed	`NCT03183856` - Comparison of Ambulatory and Functional Improvement by Morning Walk	N/A
Completed	`NCT03569397` - Music Therapy Versus Control for Total Knee Arthroplasty	N/A
Terminated	`NCT02711592` - Pharmacogenomics Information in Enhancing Post-operative Total Joint Replacement Pain Management: a Pilot Study	N/A
Completed	`NCT03145493` - Effect of Suction Drains in Total Knee Arthroplasty With Tranexamic Acid	N/A
Terminated	`NCT05602701` - Preoperative Prediction of Postoperative Physical Function
Recruiting	`NCT03570944` - Postoperative Outcomes Within an Enhanced Recovery After Surgery Protocol (POWER2)
Completed	`NCT02773537` - Motor-Sparing Peripheral Nerve Blockade Facilitates Mobility Post Total Knee Arthroplasty: A Randomized Controlled Trial	N/A
Withdrawn	`NCT02553122` - The Combined Efficacy of Evicel and Tranexamic Acid on Total Knee Arthroplasty	Phase 3
Recruiting	`NCT02385383` - An Intravenous Iron Based Protocol for Preoperative Anaemia in Hip and Knee Surgery - An Observational Study	N/A
Completed	`NCT02121392` - Epidural Catheter With or Without Adductor Canal Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty	N/A
Terminated	`NCT02155712` - Triathlon Tritanium Knee Outcomes Study	N/A