clinical trial · NCT03312465
Anatomical Shoulder Domelock System Study
Zimmer Biomet·—·active not recruiting·n = 73
Avascular NecrosisRevision SurgeryConditions Consequent to Earlier OperationsArthritis, RheumatoidArthritis, DegenerativeArthritis;TraumaticAS Domelock System
brief summary
The objectives of this study are to confirm safety and performance of the Anatomical Shoulder Domelock System when used in hemi or total shoulder arthroplasty by analysis of standard scoring systems, radiographs and adverse event records.
started
Sep 28, 2017
primary completion
Dec 9, 2032
completion
Dec 9, 2032
last updated
Mar 25, 2026
detailed description
This study is a multicenter, prospective and retrospective, non-controlled PMCF study involving orthopaedic surgeons skilled in hemi and total shoulder arthroplasty procedures. A minimum of six study centers will be involved and a total number of 73 implants will be included into the study.
official title
Anatomical Shoulder™ Domelock System A Multicenter, Prospective and Retrospective, Non-Controlled Post-Market Clinical Follow-up Study
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol