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Shoulder Arthroplasty clinical trials

View clinical trials related to Shoulder Arthroplasty.

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NCT ID: NCT05699031 Recruiting - REHABILITATION Clinical Trials

Shoulder Prosthesis Telerehab Care Trial

PROTECT
Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the rehabilitation by use of a smartphone-app with the usual care of physical therapy in patients, 60 years and older, who underwent a primary shoulder arthroplasty. The main questions it aims to answer are: - is the outcome of rehabilitation with the app as good as the usual care? - is the outcome for both types of shoulder arthroplasty similar? - what is the usability of the app?. Participants will - have treatment according to the group they are allocated to - fill in questionnaires at specific moments during the rehabilitation stage (0 - 3 months ) and at 1 year post-surgery

NCT ID: NCT03511586 Recruiting - Clinical trials for Shoulder Arthroplasty

Total Shoulder Arthroplasty Multi-Center Registry

Start date: July 28, 2015
Phase:
Study type: Observational [Patient Registry]

The objective of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.

NCT ID: NCT03268837 Recruiting - Pain Management Clinical Trials

Programmed Intermittent Bolus During Continuous Interscalene Nerve Block for Shoulder Arthroplasty

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

A new infusion strategy named the 'programmed intermittent bolus' (PIB) technique delivers the hourly dose within minutes compared to the traditional infusion that delivers such dose over an hour. The PIB technique has demonstrated superior patient satisfaction and reduced local anesthetic consumption when utilized for pain control during labour and delivery. However, it is not known if the PIB technique gives any benefits during a continuous nerve block in other settings. The aim of this randomized controlled trial (RCT) is to elucidate if PIB is better than (traditional) continuous infusion for postoperative analgesia in patients receiving a continuous nerve block for total shoulder arthroplasty with respect to pain control.

NCT ID: NCT00527839 Recruiting - Clinical trials for Shoulder Arthroplasty

Hospital for Special Surgery Shoulder Arthroplasty Cohort

Start date: April 2007
Phase:
Study type: Observational

Total joint replacements are some of the most successful medical devices developed over the last fifty years. They enable millions of people to remain ambulatory and pain free, with minimal risk. In 2002, over 200,000 total hip replacements, 350,000 total knee replacements, and 25,000 total or partial shoulder replacements were performed in the United States (HCUP data). Future use will likely be even higher: it is estimated that by the year 2020, the population 65 and over in developed countries will increase by 71%. Existing studies do not provide adequate prospective data to evaluate long-term outcomes. HSS is a world leader in total joint replacement including total shoulder arthroplasty. However, there is no systematic follow-up or evaluation of patients who have their shoulders replaced here. The purpose of this study is to establish a prospective cohort of HSS total shoulder arthroplasty to evaluate predictors of outcome, causes of failure and to allow ongoing evaluation of the results of our patients over time.