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Rotator Cuff Injuries clinical trials

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NCT ID: NCT05919121 Recruiting - Clinical trials for Subacromial Impingement Syndrome

Effect Of Hydrocortisone Phonophoresis Versus Iontophoresis In Patients With Subacromial Impingement Syndrome

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

The purpose of this study will be to compare the efficacy of adding hydrocortisone phonophoresis or iontophoresis on pain, function, range of motion and shoulder external rotation isometric strength in patients with subacromial impingement syndrome.

NCT ID: NCT05917483 Completed - Clinical trials for Rotator Cuff Injuries

Evaluation of Mechanical Characteristics of Tendons of Athletes Using Sonography

Start date: January 14, 2021
Phase:
Study type: Observational

The investigators analyzed the strain of the rotator cuff tendon of baseball pitchers obtained using ultrasonography and compared the change in peak tendon strain before and after the regular season.

NCT ID: NCT05913050 Recruiting - Clinical trials for Rotator Cuff Injuries

Predicting ROtator Cuff Tears Outcomes After Physical Therapy Treatment

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

The aim of this multicenter non-controlled study is to develop a multivariable prediction model of pain/disability improvements in patients with full-thickness rotator cuff tears, after a physical therapy treatment based on therapeutic exercise and education.

NCT ID: NCT05909930 Recruiting - Clinical trials for Rotator Cuff Injuries

Effectiveness of TheRApeutic ExercIse aNd EDucation on Patients With Massive Rotator Cuff Tears

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

The aim of this multicenter non-controlled study will be to evaluate the effectiveness of a physical therapy treatment based on resistance exercise and education for patients with massive rotator cuff tears.

NCT ID: NCT05906004 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Retrospective Data Collection and Prospective Clinical Investigation for the Augmentation or Reinforcement of the Rotator Cuff Using the Pitch-Patch

Start date: November 2024
Phase:
Study type: Observational [Patient Registry]

This is a clinical investigation study. It will verify the long-term safety and performance of the Pitch-Patch when implanted to reinforce partially repairable rotator cuff tears and used as described by the manufacturer's instructions. The medical device in this study is already on the market and is manufactured by Xiros Ltd. The Pitch-Patch is a single-use polyester prosthesis available in two sizes (30x20mm and 35x25mm). It is reinforced around the perimeter and around each eyelet to provide strength and stability to the device and repair. The study will collect data on patients who meet the entry criteria and have received the device. This is a single-armed study, meaning all patients will have a Pitch-Patch. The total length of the is expected to be 4 years; this includes a recruitment period of 2 years, and a follow-up period (for the prospective clinical investigation) of 2 years. A minimum of 32 patients will be enrolled into the study. Follow-up data will be collected at (if available for retrospective data) 3 months, 6 months, 1 year, 2 years and final follow-up (maximum 2.5 years for prospective study; maximum of 5 years for retrospective study).

NCT ID: NCT05904249 Completed - Shoulder Pain Clinical Trials

Telerehabilitation in Individuals With Rotator Cuff Tear

Start date: February 7, 2022
Phase: N/A
Study type: Interventional

The majority of patients presenting with shoulder pain are those with rotator cuff problems. Although telerehabilitation is a promising field in many areas, there is still limited high-quality research with strong evidence of its effectiveness for musculoskeletal problems. In this study, online rehabilitation and face-to-face rehabilitation will be compared in people with partial rotator cuff tears.

NCT ID: NCT05897866 Completed - Rotator Cuff Tear Clinical Trials

Sayed Issa's Hybrid Shoulder Arthroscopic-Open Surgical Management (HSSM)

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

Sayed Issa's Hybrid Shoulder Arthroscopic-Open Surgical Management (HSSM) is a limited lateral approach to the shoulder arthroscopically guided. Which achieves less surgical trauma and smaller surgical incision than even in Mini Lateral Shoulder Approach (MLSA).

NCT ID: NCT05896475 Recruiting - Rotator Cuff Tears Clinical Trials

Risk Factors for Asymptomatic Rotator Cuff Tears to Become Symptomatic.

Start date: June 2, 2023
Phase:
Study type: Observational [Patient Registry]

In this prospective study, subjects older than 55 years with a degenerative asymptomatic rotator cuff tears will be followed for a period of 2 years. After testing, a symptom registration form will be filled in every 3 months. The test moment consists of pain measurements (pain pressure thresholds and conditioned pain modulation), biomechanical measurements (strength (including hand grip strength), range of motion, ultrasound (while measuring electromyographic activity) and shear wave elastography) and psychosocial measurements (psychosocial questionnaires).

NCT ID: NCT05894265 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Prospective Study to Determine the Safety and Effectiveness of a Connective Tissue Allograft Active Matrix (AM) vs. Standard of Care in Arthroscopic Rotator Cuff Repair

Start date: June 5, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to see how well the ActiveMatrix® graft works at improving healing and function of the shoulder following rotator cuff repair surgery

NCT ID: NCT05886296 Recruiting - Surgery Clinical Trials

Pre-surgical Information Session for People Who Must Undergo Shoulder Rotator Cuff Surgery

Start date: May 19, 2023
Phase: N/A
Study type: Interventional

The shoulder is the most mobile joint in the human body. Movements are carried out in most of the activities we participate in, such as work, sports, household tasks, shopping and leisure activities. Shoulder diseases affect 21% of the western population and is one of the most frequent reasons for consultation in orthopedics and rehabilitation consultations. Shoulder pain is in a large majority of cases related to the slope of the acromion and rotator cuff pathology, which would include the slope of the acromion syndrome. The degree of involvement can range from bursitis, tendinitis, to tendinous ruptures. Initial treatment is usually conservative and may consist of anti-inflammatory medication and rehabilitation. When the pain is not relieved, surgery is usually recommended. Surgery for rotator cuff tears is increasingly performed minimally invasive, using arthroscopy. Hospital admission days are currently being reduced, so many of the scheduled shoulder surgeries are performed via the Outpatient Surgery Unit. Often, users are not seen again by the surgeon until a week after the intervention. The affected person must empower themselves and participate actively and progressively in their recovery process. This process begins right after the surgical intervention. Therefore, it is very important that the person has all the necessary information about the surgical procedure that has been performed. Patient education is crucial to reduce anxiety and optimize surgical outcomes.