Actively Recruiting
To Evaluate the Safety and Clinical Radiological Outcomes in 2 Years of Embrance Model Reverse Shoulder Arthroplasty
Led by Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal · Updated on 2024-09-19
250
Participants Needed
1
Research Sites
240 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The use of inverted prostheses to replace shoulder joints damaged by degenerative or traumatic processes has become widespread over the past three decades. Current designs, used correctly, can restore function and improve pain in the majority of patients in whom they are implanted. The aim is to carry out a more detailed follow-up of the subjects who are implanted with this prosthetic model on a primary basis, analysing the clinical and radiological results and evaluating the presence of adverse effects of the prosthesis or short-term complications. For this purpose, subjects will be closely monitored for two years.
CONDITIONS
Official Title
To Evaluate the Safety and Clinical Radiological Outcomes in 2 Years of Embrance Model Reverse Shoulder Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who give their written consent to participate after being informed about the study
- Age over 18 years
- Have a shoulder joint disorder treatable with Embrace reverse arthroplasty
- Have a CT or MRI scan done within 6 months before surgery
You will not qualify if you...
- Patients who have had any type of arthroplasty on the same shoulder
- Patients with an active infection anywhere at the time of shoulder surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Miguel Ángel Ruiz Ibán
Madrid, Spain, 28034
Actively Recruiting
Research Team
M
Miguel Ángel Ruiz Iban, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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