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Shoulder Disease clinical trials

View clinical trials related to Shoulder Disease.

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NCT ID: NCT06070909 Completed - Shoulder Disease Clinical Trials

Selective Activation of the Infraspinatus During External Rotation Exercises in Participants With Rounded Shoulder Posture

Start date: July 15, 2023
Phase:
Study type: Observational

The purpose of this prospective, cross-sectional study was to evaluate the selective activation of the infraspinatus during external rotation exercises in participants with rounded shoulder postures and compare the different exercise positions. The fifteen (7 males and 8 females) participants with rounded shoulder posture were recruited for this study. The EMG activations of the middle trapezius, posterior deltoid and infraspinatus muscles in the dominant limb were recorded during exercises in standing external rotation (SER), side-lying position (SDER), scapular plane (SPER) and muscle architecture-based (MABER) positions.

NCT ID: NCT05370872 Completed - Clinical trials for Musculoskeletal Injury

Efficacy of a Remotely Administered Functional Capacity Test on Return-to-work Outcomes

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

Currently, injured workers are required to visit a clinic, in-person, for functional testing as part of the rehabilitation and return-to-work process. The need for in-person testing has always caused problems for workers in remote areas without easy access to clinics. COVID-19 has made the problem of access to in-person clinical testing worse. Now, many injured workers can't receive functional testing due to COVID-19 related clinic closures and isolation restrictions. The investigators aim to develop and evaluate a functional testing protocol that can be delivered remotely to solve the problem of access to in-person clinic testing. A functional test that can be completed remotely, while the client remains in their home will increase access to timely testing, improve client satisfaction by removing the need for costly and time consuming travel, and will continue to help injured workers quickly recover and return to meaningful work. This research study will help to determine if return-to-work outcomes improve, or remain unchanged, when functional testing is completed remotely relative to in the clinic.

NCT ID: NCT05153863 Completed - Shoulder Injuries Clinical Trials

C Scope Visualization System Prospective Study

Start date: January 20, 2022
Phase: N/A
Study type: Interventional

Evaluation of the performance and safety of the C Scope Visualization System

NCT ID: NCT04185064 Completed - Shoulder Injuries Clinical Trials

Cryopneumatic Device After Shoulder Surgeries

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

This study randomize patients to receive either a cryopneumatic device or standard care (ice and ice packs) following open or arthroscopic shoulder surgeries. The primary objective is to determine the impact of the cryopneumatic device on post-surgery pain management, while secondary objectives are to detemine the effect on pain, patient eperience, quality of life, narcotic consumption and time to stop narcotic usage. Patients who do not wish to participate in the randomized portion of the trial will be invited to participate in an observational cohort who will all receive the cryopneumatic device. Patients who wish to enter this cohort will not have the device provided to them for free, and will either use their insurance or pay for the device, in order to determine if patients who pay demonstrate different outcomes from the patients receiving the device for free in the RCT.

NCT ID: NCT03956316 Completed - Shoulder Disease Clinical Trials

Short-Term Outcomes of Total Shoulder Arthroplasty Using the Titan Modular Total Shoulder System

Start date: October 15, 2014
Phase:
Study type: Observational

The goals of total, reverse total and hemi shoulder arthroplasty are the same, to alleviate the patient's pain and obtain a full functional recovery. This outcome depends on the surgeon's ability to reproduce normal glenohumeral anatomy including bone morphology, capsular tension and rotator cuff function. Shoulder arthroplasty has become a safe and effective treatment for various diseases of the shoulder. This study goal is to document and report the short-term functional, radiographic, and quality of life outcomes of total shoulder arthroplasty (TSA) using the titan modular shoulder system.

NCT ID: NCT03877835 Completed - Shoulder Disease Clinical Trials

Diaphragm-sparing Nerve Blocks for Shoulder Arthroplasty

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

The combination of a modified lateral sagittal infraclavicular block and a suprascapular nerve block has not been studied in a cohort of total arthroplasty patients. Such diaphragm-sparing nerve blocks for shoulder arthroplasty may provide a very good anesthetic alternative in lung diseased patients who are in need for total arthroplasty of the shoulder.

NCT ID: NCT03393559 Completed - Cerebral Ischemia Clinical Trials

Effect of Leg Elevation on Prevention of Intraoperative Hypotension During Beach Chair Position

Start date: January 24, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of leg elevation on the prevention of intraoperative hypotension during shoulder surgery in the Beach-chair position. patients undergoing shoulder surgery in the Beach-chair position will be randomly assigned to Group L (with leg elevation) or Group C (no intervention). The primary outcome is the incidence of intraoperative hypotension (mean blood pressure < 60mmHg or systolic blood pressure < 80% of baseline). Secondary outcomes are the incidence of intraoperative cerebral desaturation (cerebral oxygen saturation < 80% of baseline, longer than 30 seconds), total amounts of administered inotropic agents, and systolic blood pressure, heart rate, and cerebral oxygen saturation at various time points.

NCT ID: NCT03329456 Completed - Anesthesia Clinical Trials

MEV to Block the Posterior and Lateral Cords of the Infraclavicular Brachial Plexus

LSIB
Start date: October 30, 2017
Phase: Phase 4
Study type: Interventional

The investigators have recently shown that LSIB in combination with a suprascapular and a cervical plexus block is a very good alternative for arthroscopic shoulder surgery. However, the investigators believe the total volume of local anesthetic for LSIB may be reduced. For shoulder surgery there is no need to block the medial cord and the investigators therefore hypothesize a significantly lower MEV95% by applying a selective lateral and posterior cord block