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Rotator Cuff Tear clinical trials

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NCT ID: NCT03577379 Completed - Rotator Cuff Tear Clinical Trials

Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The goal of this study is to assess whether undergoing surgical repair of the rotator cuff with the additional intervention of whole blood fibrin clot will improve rotator cuff vascularization at the bone-tendon interface repair site and patient outcomes compared to those who do not receive the whole blood fibrin clot intervention.

NCT ID: NCT03573765 Completed - Osteoarthritis Clinical Trials

Epidemiology and Outcomes of Upper Limb Surgery: Analysis of Routine Data

Start date: April 6, 1998
Phase:
Study type: Observational

Surgery is a common treatment type for damaged joints, tendons and nerves in the upper limb where conservative measures are inappropriate or have failed. These conditions are common and result in significant levels of pain and functional disability. The investigators are conducting a broad ranging study of variation in the provision of surgical treatment and factors affecting outcomes after surgical treatment of upper limb conditions. This will be a population-based study of all patients undergoing surgical treatment funded by the National Health Service (NHS) of England over a nineteen-year period. This study will help to understand the factors associated with a poor outcome following surgery, which can be shared with patients considering treatment options. The investigators will also document current and future health service burden associated with commonly performed surgical procedures including complications and repeat operations.

NCT ID: NCT03567954 Terminated - Rotator Cuff Tear Clinical Trials

The Accuracy of Ultrasound in Detecting Rotator Cuff Tears in Proximal Humerus Fracture Patients

Start date: June 22, 2018
Phase:
Study type: Observational

The aim of this study is to determine the diagnostic accuracy of ultrasonography (US) in detecting full-thickness (a lesion that extends through both the bursal and articular part of the tendon) rotator cuff tear in patients who have sustained a proximal humerus fracture, using operative examination as the golden standard.

NCT ID: NCT03551509 Active, not recruiting - Rotator Cuff Tear Clinical Trials

LifeNet: Extracellular Matrix Graft in Rotator Cuff Repair

Start date: July 1, 2018
Phase: Phase 4
Study type: Interventional

This trial is to evaluate the effectiveness of the ArthroFLEX® ECM scaffold graph as an augment in rotator cuff repair surgery to reduce the failure rate of rotator cuff repairs for large and massive rotator cuff tears.

NCT ID: NCT03548662 Completed - Rotator Cuff Tear Clinical Trials

The Effect of Platelet Rich Plasma Injection Combined With Exercise Rehabilitation in Patients With Rotator Cuff Tear

Start date: March 4, 2014
Phase: Phase 1
Study type: Interventional

This study aims to evaluate the effect of platelet rich plasma combined with exercise therapy for patients with partial thickness rotator cuff tears.

NCT ID: NCT03540030 Completed - Opioid Use Clinical Trials

Opioid-Free Shoulder Arthroplasty

Start date: September 2016
Phase: Phase 4
Study type: Interventional

Purpose of Study: To identify and provide a safe, opioid-free treatment pathway for shoulder arthroplasty with a focus on perioperative pain control and postoperative symptoms from treatment

NCT ID: NCT03533088 Completed - Rotator Cuff Tear Clinical Trials

Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Start date: July 15, 2019
Phase: N/A
Study type: Interventional

Rotator cuff (RC) repair is one of the most common treatment approch to relief the pain and improve the shoulder function on patients with rotator cuff rupture. Despite the improved surgical techniques and decreased failure rate, there are still complications after the surgey like shoulder persistant shoulder pain, stiffness even re-tear. Therefore, rehabilitation after the RC repair procedure is crucial for the success of the treatment. However, there is no concencus between the post-operative rehabilitation protochol. The aim of this study is to compare two different rehabilitation protochols on patients with RC repair.

NCT ID: NCT03525275 Completed - Pain, Postoperative Clinical Trials

Effect of Battlefield Acupuncture and Physical Therapy Versus Physical Therapy Alone After Shoulder Surgery

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

The purpose of this randomized clinical trial is to determine the effectiveness of Battlefield Acupuncture (BFA) in addition to usual post-surgical shoulder physical therapy compared to a standard shoulder rehabilitation program in reducing medication use and pain in patients who have undergone shoulder surgery. Measurements of medication (opioid, NSAID, acetaminophen, etc.) use (daily number of pills consumed), pain rating, patient specific functional scale and global rating of change will be taken at 24, 72 hours, 7 days, 14 days and at six weeks post-surgery. It is hypothesized that the inclusion of Battlefield Acupuncture will result in a decrease in medication use and post-surgical pain when compared to rehabilitation alone. The population for this study is male and female DoD beneficiaries, ages 17-55 (17 if cadet) that are not participating in other shoulder research studies. The subjects in the experimental group will receive Battlefield Acupuncture in addition to their respective post-surgical shoulder rehabilitation protocol.

NCT ID: NCT03488433 Withdrawn - Rotator Cuff Tear Clinical Trials

Abduction Brace Versus Antirotation Sling for Immobilization Following Reverse Shoulder Arthroplasty and Rotator Cuff Repair

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

To compare the functional and anatomical outcomes, and patient satisfaction and compliance between two different postoperative immobilization methods - abduction shoulder brace versus simple arm sling - following 2 common shoulder surgical procedures - rotator cuff repair (RCR) and reverse total shoulder arthroplasty (RTSA) through a prospective randomized clinical trial.

NCT ID: NCT03431857 Completed - Clinical trials for Rheumatoid Arthritis

Multi Centre Study on TESS V2 Shoulder System

Start date: October 20, 2010
Phase:
Study type: Observational

This study is a Post Market Clinical Follow-up study to fulfill the post market surveillance requirements. The data collected from this study will serve the purpose of confirming safety and performance of the TESS Shoulder System.