The Evaluation of the METS™ Proximal Humeral System

Status Completed

Clinical Trial Summary

This study is a single centre, non-randomised, post market clinical follow up examining retrospective patient data from a series of surgical cases; which involved the endoprosthetic replacement of the proximal humerus using the Stanmore Implant Worldwide METS (Modular Endoprosthetic Tumour System) Proximal Humeral system.

The objective of this study is to evaluate the retrospective patient data where patients have been followed up for at least 12 months post operation; to demonstrate the safety of the METS Proximal Humeral replacement system.

Clinical Trial Description

The METS™ Proximal Humeral system is an endoprosthetic replacement designed to restore the length and the function of an arm after the resection of a significant amount of bone tissue; due to a malignant tumour in the proximal humerus. This Post Market Clinical Follow up (PMCF) study is designed to further support the existing evidence that the system is safe and performs as expected, when analysing retrospective patient data that have had a METS™ Proximal Humeral replacement. The target population is male or female subjects aged between 18 years and over who have been implanted with a METS™ Proximal Humeral system at the Royal National Orthopaedic Hospital, Stanmore; and the patient has been followed up for at least 12 months following implantation. ;

Study Design

Related Conditions & MeSH terms

Complications; Arthroplasty

Clinical Trial Details

NCT number	NCT02774174
Study type	Observational
Source	Stryker Orthopaedics
Contact
Status	Completed
Phase
Start date	May 2016
Completion date	December 2016

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT02043132` - Tranexamic Acid in Reverse Total Shoulder Arthroplasty	Phase 2/Phase 3
Recruiting	`NCT02255331` - Using MRI To Detect Soft Tissue Reactions And Implant Integration As Related To Implant Modularity
Completed	`NCT01442298` - A Comparison Between an Individual Low Tourniquet Pressure Versus a Standard Pressure During Total Knee Arthroplasty	N/A
Withdrawn	`NCT02054936` - Evaluation of Wound Drainage After Knee or Hip Arthroplasty	Phase 4
Recruiting	`NCT01542580` - A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee
Completed	`NCT01882751` - In Vivo Comparison of Knee Kinematics for Subjects Implanted With Either a ConforMIS or Traditional Knee Implant
Completed	`NCT02598700` - Correlation of Spinopelvic Parameters and Acetabular Cup Orientation
Completed	`NCT01820611` - Arcos Revision Stem: Evaluation of Clinical Performance
Completed	`NCT01514318` - Encore Revelation Hip Stem	N/A
Completed	`NCT02124031` - Mexican Initiative of Patients With Osteoarthritis and Rheumatoid Arthritis (IMPACTAR)	N/A
Completed	`NCT01373112` - Articulating Versus Static Antibiotic Loaded Spacers for the Treatment of Prosthetic Knee Infection	N/A
Completed	`NCT01373099` - Study of Antibiotic Spacer Design to Treat Infection After Hip Replacement	N/A