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Rotator Cuff Injuries clinical trials

View clinical trials related to Rotator Cuff Injuries.

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NCT ID: NCT05320419 Completed - Rotator Cuff Tear Clinical Trials

The Effect of Amniotic Membrane Injection as An Addition to Physical Therapy in Patients With Rotator Cuff Tear

Start date: March 29, 2023
Phase: N/A
Study type: Interventional

Rotator cuff tear (RCT) is a commonly seen pathology in shoulder disease, which causes significant disability in daily living and work. Based on a cohort study of a large population, the prevalence of rotator cuff full-thickness tear was 20.7%. More broadly, the prevalence of rotator cuff abnormalities increased with age and up to 62% in population more than 80 years old. The pathophysiology of RCT could be attributed to extrinsic factors such as impingement by surrounding tissue and intrinsic factor such as tendon degeneration. According to previous study using histochemical and immunocytochemical techniques, fibrocartilaginous metaplasia, decreasing vascularity and fibroblast numbers were found in rotator cuff tear. Besides, the inflammatory response diminished as the tear size increased. The treatment of RCT includes surgery and non-operative treatment. The prognosis depends on the symptoms, tear size, chronicity and other structures involvement. Previous meta-analysis study reported that the effectiveness between surgery and conservative treatment is similar in treating RCT. Therefore, relative rest, oral medication, physical therapy and injection therapy were commonly used in first-line treatments. When treating shoulder pain with injection therapy, steroid was often used at first for short-term pain relief and anti-inflammation. However, the potential cytotoxic effect was found and could be harmful in tendon repair. To accelerative the healing process of soft tissue injury, regenerative injection become more popular and expectable over past few years. A meta-analysis study reported the positive long-term effect of prolotherapy and platelet-rich plasma (PRP). More recently, bone marrow concentrate (BMC) and amniotic membrane (AM) have been used in soft tissue repair and many clinical studies are processing.

NCT ID: NCT05318209 Recruiting - Clinical trials for Shoulder Impingement Syndrome

Effect of Closed-chain Shoulder Girdle Scapular Depression Exercise on Shoulder Impingement Syndrome

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule & pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule & pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound . The exercise program will consist of 3 sessions / week for 5 weeks

NCT ID: NCT05300607 Recruiting - Clinical trials for Rotator Cuff Injuries

The Western Ontario Rotator Cuff Index Arabic Version

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

To evaluate, translate, culturally adapt, validate, and investigate the reliability of Arabic version of The Western Ontario Rotator Cuff Index (WORC). The null hypothesis of this study will be stated as: Arabic language version of the WORC doesn't have face, content, or construct validity enough to measure quality of life related to rotator cuff disorders in Arabic patients. Arabic language version of the WORC doesn't have reliability to measure quality of life related to rotator cuff disorders in Arabic patients

NCT ID: NCT05297305 Recruiting - Clinical trials for Rotator Cuff Injuries

Onlay Versus Inlay Humeral Component in Reverse Total Shoulder Arthroplasty

Start date: October 20, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to compare the effect of different ways to place the component that goes at the top of the humerus (upper arm) in reverse total shoulder replacement. Some surgeons place the humeral tray component sitting on the bone while others place it in the bone. Changing the way that the humeral component is placed may change how much the arm can raise up or turn out/in after surgery for some patients. This study compares patients with inlay humeral component (tray sits in the upper arm bone) versus onlay humeral component (tray sits on top of the upper arm bone) to see if there are differences in range of motion or function after surgery.

NCT ID: NCT05277077 Completed - Clinical trials for Rotator Cuff Injuries

Pain Neuroscience Education Following Arthroscopic Rotator Cuff Repair

Start date: March 31, 2022
Phase: N/A
Study type: Interventional

Pain neuroscience education (PNE) aims to explain to patients the biological and physiological processes involved in a pain experience and, more importantly, defocus the issues associated with the anatomical structures. It has been demonstrated for musculoskeletal pain, PNE provides compelling evidence in reducing pain, disability, pain catastrophization, and limited physical movement. Rotator cuff tears (RCT) often lead to pain aggrevation, deterioration of patients' functioning and considerable economic burden for health care resources requiring consultations, physiotherapy, radiological examinations and surgery. Despite costly arthroscopic surgeries and long-term physiotherapy treatments, satisfactory results are scarce. The lack of satisfactory results at the end of all this effort suggests that some practices should be revised. Although PNE is likely to have beneficial effects on shoulder pathomechanics, to our knowledge, there is no randomized controlled research in the relevant literature investigating the effects of PNE in patients with an RCT. The present study aims to examine the effectiveness of PNE on clinical outcomes in a sample of patients with RCT.

NCT ID: NCT05274737 Recruiting - Rotator Cuff Tears Clinical Trials

Comparison Of A Novel Sling With A Traditional Abduction Sling After Shoulder Surgery

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

The objective of this study is to determine if the novel shoulder sling has higher patient satisfaction compared to a traditional, abduction sling with at least equivalent postoperative outcomes after arthroscopic rotator cuff repair and total shoulder arthroplasty.

NCT ID: NCT05266391 Completed - Clinical trials for Subacromial Impingement Syndrome

Injection Technique in Subacromial Impingement Syndrome

SAIS
Start date: June 1, 2018
Phase:
Study type: Observational

Since pain is usually accompanied by a substantial effect on daily life that results in the extensive use of healthcare resources. In subacromial impingement syndrome, shoulder pain affects the quality of life negatively by affecting upper extremity functions and interrupting night sleep. It is very important to control the pain in order to reduce the loss to the labor force and prevent the pain from becoming chronic. Various physical treatment methods such as ultrasound, hot pack, transcutaneous electrical nerve stimulation, etc., and injections or medical agents are recommended. This study aimed to compare the effects of ultrasound (US)-guided in comparison to landmark guided subacromial corticosteroids injection on shoulder range of motion (ROM), pain, and functional status in patients with subacromial impingement syndrome (SAIS).

NCT ID: NCT05266352 Completed - Rotator Cuff Tears Clinical Trials

Investigation of the Effect of Exercise Training on Psychosocial Outcomes in Rotator Cuff Tears

Start date: February 28, 2022
Phase: N/A
Study type: Interventional

This study aimed to determine the psychosocial effects of exercise training in patients with rotator cuff tears.

NCT ID: NCT05266339 Enrolling by invitation - Surgery Clinical Trials

Cross-education in Arthroscopic Rotator Cuff Repair: A Randomized Controlled Trial

Start date: May 9, 2022
Phase: N/A
Study type: Interventional

This randomized-controlled trial aims to investigate the efficacy of cross-education on function, pain, and range of motion, muscle strength and quality of life in patients who underwent arthroscopic rotator cuff repair.

NCT ID: NCT05264935 Recruiting - Clinical trials for Rotator Cuff Tendinitis

Ultrasound-guided Lavage of Calcific Deposits of the Rotator Cuff

Kalklavage
Start date: May 1, 2022
Phase:
Study type: Observational

The primary goal of the study is to assess ultrasonographic Power Doppler signals after ultrasound-guided puncture and lavage of rotator cuff calcific tendinitis of the shoulder. Secondary outcomes are sonographic features like the course of residual calcific material and the course of tendon healing als well as the clinical symptoms of the patient.