Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study
NCT: NCT05868148 · ACTIVE_NOT_RECRUITING
Brief Summary
The goal of the Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study is to collect safety and performance data on the commercially available Shoulder iD™ Primary Reversed Glenoid device. The study will learn about standard device use in adult patients who have a functional deltoid muscle and massive and non-repairable rotator cuff tear. The main questions it aims to answer are: * What is the average improvement in patient-reported shoulder function after 2 years when compared to before the surgery, and * What is the rate of surgical revisions needed over a 10 year period Patients will be asked to will be asked to regularly attend their check-up visits with their surgeon (including having x-rays or CT images taken to check their shoulder and implant), to complete questionnaires to report how their shoulder is doing, and to tell their surgeon when they notice any changes.
Frequently Asked Questions
What is Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study?
Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study is a clinical trial registered under NCT05868148. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT05868148?
The current status of NCT05868148 (Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study) is: ACTIVE_NOT_RECRUITING.
When did Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study start?
Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study started on 2023-10-20.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.