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Rotator Cuff Injuries clinical trials

View clinical trials related to Rotator Cuff Injuries.

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NCT ID: NCT06055478 Recruiting - Rotator Cuff Tears Clinical Trials

Effect of Suprascapular Nerve Block and Axillary Nerve Block After Arthroscopic Rotator Cuff Repair

Start date: September 25, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to verify the effect of suprascapular nerve block and axillary nerve block in relieving postoperative pain after arthroscopic rotator cuff repair. Are there differences in visual analog pain scale and patient's satisfaction? Are there differences in mean plasma pain related cytokines? The participants will undergo preemptive ultrasound guided suprascapular nerve block and axillary nerve block using each 0.75% ropivacaine 10mL or each 0.9% saline 10mL.

NCT ID: NCT06039345 Recruiting - Shoulder Pain Clinical Trials

Shoulder RFA Pilot Study

Start date: February 7, 2024
Phase:
Study type: Observational

Through this prospective, single-arm cohort pilot study, we plan to explore the safety and effectiveness of Shoulder Radiofrequency Ablation (SRFA) in patients with non-operative chronic shoulder pain due to shoulder osteoarthritis with or without rotator cuff tears.

NCT ID: NCT06024551 Recruiting - Clinical trials for Rotator Cuff Injuries

Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy

Start date: December 15, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to investigate the effect of telerehabilitation in patients with rotator cuff tendinopathy. The main questions it aims to answer are: - Is telerehabilitation effective in improving the functional status of patients with rotator cuff tendinopathy? - Is telerehabilitation effective in reducing the pain of rotator cuff patients?

NCT ID: NCT05988541 Recruiting - Rotator Cuff Tears Clinical Trials

Rotator Cuff Integrity and Clinical Outcomes 5 Years After Repair.

Start date: October 3, 2023
Phase: N/A
Study type: Interventional

The study gives an overview of surgically treated rotator cuff injury patients in Tartu University Hospital Sports Traumatology Centre during 2013-2019 and evaluates the integrity of rotator cuff at minimum 5 years after atraumatic rotator cuff tendon repair. First stage of the study describes the study population, etiology of the injury (traumatic/atraumatic) and aims to answer the question whether the arthroscopic findings are in line with the preoperative imaging studies or not. Second stage of the study focuses on atraumatic tendon tears assessing structural integrity of the tendons 5 years after repair using ultrasound imaging. The main question is - does the findings correlate with clinical outcomes and patient satisfaction. Participants of the second phase of the study will be asked for an appointment to have their shoulders examined with ultrasonography and clinical outcomes are measured using the American Shoulder and Elbow Surgeons (ASES) Score, The Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire and The Constant-Murley score (CMS).

NCT ID: NCT05981833 Recruiting - Clinical trials for Full-thickness Rotator Cuff Tear

Dermal Allograft Augmentation of Large and Massive Rotator Cuff Tears

Start date: September 25, 2023
Phase:
Study type: Observational

The purpose of this study is to compare postoperative healing of large and massive rotator cuff tears with preoperative MRI confirmed fatty infiltration stage II and higher repaired with or without dermal allograft augmentation (DAA).

NCT ID: NCT05966298 Recruiting - Clinical trials for Subacromial Impingement Syndrome

Investigation of the Effectiveness of Core Stabilization Training in Patients With Subacromial Impingement Syndrome

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

Subacromial Impingement Syndrome (SSS) is one of the most common shoulder problems. The core region is considered a kinetic link that facilitates the transfer of torque and angular momentum between the upper and lower extremities during body movements. The decrease in core stabilization affects both trunk control and the quality of extremity movements depending on the kinetic chain in the body. The improvement in core stabilization balances the load transfer between the trunk and the extremities and reduces the asymmetry between the extremities. Core stabilization training should be included in rehabilitation programs as core stabilization is adversely affected in patients with CNS. For this reason, this study was planned to examine the effects of core stabilization training applied in addition to conventional treatment in patients with CNS on pain, range of motion, upper extremity function and core stability.

NCT ID: NCT05959733 Recruiting - Rotator Cuff Tears Clinical Trials

Maximal Repair Versus Bridging Reconstruction With BioBrace®

Start date: December 7, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if using BioBrace® to reconstruct the gap in the rotator cuff tears lead to better results for patients compared to the traditional maximal repair method. This study will use a variety of clinical, radiographic, and functional outcome measures. Specifically, the researchers will be comparing the re-tear rate, patient reported outcomes, shoulder strength, range of motion, muscle activation, in-vivo biomechanics, and other radiographic outcomes using x-ray and MRI.

NCT ID: NCT05946343 Recruiting - Shoulder Pain Clinical Trials

Rotator Cuff Tear Severity and Scapular and Rotator Cuff Muscle Activation Patterns

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

Rotator cuff tears are common musculoskeletal injuries that can lead to altered scapular and rotator cuff muscle activation patterns and reduced function. This study aims to investigate the relationship between rotator cuff tear severity and scapular and rotator cuff muscle activation patterns. The primary objective of this study is to determine whether a relationship exists between the severity of rotator cuff tears and the activation patterns of scapular and rotator cuff muscles. Secondary objectives include: 1. Identifying differences in muscle activation patterns between varying tear sizes. 2. Evaluating the potential of these activation patterns as an indicator for the severity of rotator cuff tears. 3. Assessing the influence of muscle activation patterns on the functional capacity of the affected shoulder.

NCT ID: NCT05927935 Recruiting - Clinical trials for Femoroacetabular Impingement Syndrome

First-line Treatment for Femoroacetabular Impingement Syndrome

BetterHip
Start date: July 1, 2023
Phase: N/A
Study type: Interventional

There is sparse evidence on the effectiveness of first-line treatment in patients with femoroacetabular impingement syndrome (FAIS) regarding clinical- and cost-effectiveness. The goal of this randomized controlled trial is to compare the clinical effectiveness and cost-effectiveness of a supervised strength exercise intervention to usual first-line care in patients with FAIS. The main hypothesis it aims to investigate are: 1. 6-months of supervised strength exercise intervention is superior (i.e., at least 6 points, on a scale from 0-100) to usual care in improving hip related quality of life in patients with FAIS at the end of intervention. 2. 6-months of supervised strength exercise intervention is cost-effective compared to usual first-line care at 12-month follow-up in patients with FAIS. 3. High exercise adherence and dosage will be superior to low exercise adherence and dosage in mediating clinical effectiveness in patients with FAIS.

NCT ID: NCT05926622 Recruiting - Avascular Necrosis Clinical Trials

Clinical and Radiological Outcomes of Medacta Shoulder System FR

Start date: March 15, 2022
Phase:
Study type: Observational

This is a post-marketing surveillance on Medacta Shoulder System