RecruitingNot ApplicableNCT04258267

Which Factors Influence the Outcome After Anatomical and Reverse Shoulder Arthroplasty?

Which Factors Influence the Outcome After Anatomical and Reverse Shoulder Arthroplasty? A Prospective Longitudinal Study With Randomized Group Allocation, Towards Better Rehabilitation Strategies


Sponsor

Universiteit Antwerpen

Enrollment

97 participants

Start Date

Jan 14, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of this study is to investigate pre-, intra- and post-operative factors that influence post-operative outcome (shoulder pain, shoulder function and quality of life) after shoulder arthroplasty.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is collecting information from patients who are undergoing shoulder replacement surgery (shoulder arthroplasty) to understand what factors influence how well patients do afterward. There are two main types of shoulder replacement — anatomical (which replaces the shoulder joint in its natural orientation) and reverse (where the ball-and-socket are switched, often used for patients with rotator cuff problems). Researchers want to identify which patient characteristics, health conditions, and surgical details predict the best outcomes. This is an observational registry study, meaning it does not test a new treatment but instead tracks outcomes from standard surgeries. All adults scheduled for their first (primary) shoulder replacement are eligible to participate. You may be eligible if: - You are 18 years of age or older - You are scheduled for a primary (first-time) shoulder arthroplasty (either anatomical or reverse) You may NOT be eligible if: - You are having revision surgery (a repeat surgery to fix or replace a previous shoulder implant) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

PROCEDUREEarly mobilization

Patients will wear an adduction sling to immobilize the shoulder during the first 4 weeks post-operative

PROCEDUREDelayed mobilization

Patients will wear an abduction sling to immobilize the shoulder during the first 4 weeks post-operative, followed by an adduction sling for 2 weeks.


Locations(1)

AZ Monica

Deurne, Antwerp, Belgium

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04258267


Related Trials