Loading clinical trials...

Long-term Study of the DePuy Low Contact Stress (LCS) Complete Total Knee System | Clinical Trials | Clareo Health

COMPLETEDPHASE4

Long-term Study of the DePuy Low Contact Stress (LCS) Complete Total Knee System

A Prospective, Non-Comparative Study to Evaluate the Performance of the DePuy Low Contact Stress (LCS) Complete Mobile-bearing Total Knee System.

NCT00733915•DePuy International

View on ClinicalTrials.gov

Summary

The main objective of this study is to evaluate how the LCS Complete mobile-bearing total knee system and surgical instrumentation performs.

Detailed Description

The secondary objective of this investigation is to evaluate the long-term survivorship and performance of the LCS Complete mobile-bearing total knee system and surgical instrumentation using the American Knee Society Score (AKS) the Oxford Knee Score (OKS), SF-12 and survivorship analysis.

Eligibility

Age

All ages

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Male or female subjects.
•Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained
•Subjects who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
•Subjects who present with idiopathic osteoarthritis, rheumatoid arthritis, post traumatic arthritis or any other pathology that in the opinion of the clinical investigator requires a primary total knee arthroplasty and who are considered suitable for treatment with a mobile bearing knee system (LCS Complete).
•Subjects who in the opinion of the Clinical Investigator are considered to be suitable for treatment with the investigation device, according to the indications specified in the package insert leaflet.

Exclusion Criteria

•Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
•Subjects with a known history of poor compliance to medical treatment.
•Women who are pregnant.
•Subjects who are known drug or alcohol abusers or with psychological disorders that could effect follow-up care or treatment outcomes.
•Subjects involved in Medical-Legal claims.
•Subjects who have participated in a clinical study with an investigational product in the last month.
•Subjects who are currently involved in any injury litigation claims.
•Revision of an existing knee implant.

Locations (1)

Musgrave Park Hospital

Belfast, Ireland

Key Dates

Start Date

March 1, 2002

Primary Completion Date

September 1, 2007

Completion Date

October 1, 2014

Last Updated

September 12, 2025

Enrollment

241

ACTUAL participants

Conditions

Arthroplasty, Replacement, Knee

Interventions

L.C.S. Complete Knee (DePuy Low Contact Stress Complete Knee System)

DEVICE

Nurse-Led Telehealth vs In-Person Follow-Up After Total Knee Replacement

NCT07058623

Arthroplasty, Replacement, KneeOsteoarthritis, Knee

View study

RECRUITING

Multigen Plus H Study and AMF TT Cones

NCT04884542

Arthroplasty, Replacement, Knee

View study

RECRUITING

Biomechanics and Clinical Outcomes in Responders and Non-Responders

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 12, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

Long-term Study of the DePuy Low Contact Stress (LCS) Complete Total Knee System

Inclusion Criteria

Exclusion Criteria

Nurse-Led Telehealth vs In-Person Follow-Up After Total Knee Replacement

Multigen Plus H Study and AMF TT Cones

Biomechanics and Clinical Outcomes in Responders and Non-Responders

CGM Monitoring in T2DM Patients Undergoing Orthopaedic Replacement Surgery

A Study of the Effect of a Nurse Navigator Program on High Risk Patients

Systemic Lidocaine Versus Ultrasound-guided Adductor Canal Block for Patients Undergoing Total Knee Arthroplasty