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Rotator Cuff Injuries clinical trials

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NCT ID: NCT05779033 Enrolling by invitation - Clinical trials for Shoulder Impingement Syndrome

Ultrasound Versus Kinesiotaping in Shoulder Impingement Syndrome

US-SIS-KT
Start date: April 9, 2023
Phase: N/A
Study type: Interventional

studying the effect of ultrasound and kinesiotaping in shoulder impingement syndrome in reliefing pain and increase range of motion in subjects with shoulder impingement syndrome .

NCT ID: NCT05778422 Completed - Shoulder Pain Clinical Trials

Bupivacaine or Radiofrequency for Shoulder Pain

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Comparative study between pulsed radiofrequency in suprascapular nerve or bupivacaine block for chronic shoulder pain

NCT ID: NCT05770908 Recruiting - Clinical trials for Rotator Cuff Tendinitis

Multimedia Animations to Support Therapeutic Exercise for Rotator Cuff Shoulder Pain

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

The goal of this randomized controlled trial is to evaluate the benefits from adding multimedia animations to a paper-based therapeutic exercise program in subjects with rotator cuff related shoulder pain. The main question[s] it aims to answer are: - Does subjects improve more regarding shoulder disability and pain? - Are the subjects more satisfied with the treatment received? - Do the subjects adhere more to the exercise program? - Do the subjects perform better the trained exercises? - Do the subjects have greater expectations with the treatment received? Participants will perform a therapeutic exercise program within 6 months. Researchers will compare the addition of web-app animations to the classical paper-based information.

NCT ID: NCT05742581 Completed - Rotator Cuff Tears Clinical Trials

Critical Shoulder Angle and Acromial Index on 3D Models

Start date: June 1, 2019
Phase:
Study type: Observational

Objective: The relationship between rotator cuff tears and morphological features of the shoulder joint has not been fully explained. The earlier studies are usually done with two-dimensional radiography images, but joint positions and bone formations could not be fully evaluated in two-dimensional images. This study aims to evaluate the relationship between rotator cuff tears and critical shoulder angle (CSA) and acromial index (AI) values in three dimensions. Methods: This study examined computerized tomography of 24 rotator cuff tears (rotator cuff tear group) and 20 Bankart lesions, and no rotator cuff tears (control group). CSA and AI were measured on three-dimensional glenohumeral joint models obtained by three-dimensional reconstructions of computed tomography examinations. The investigators anticipate results of this study will guide clinicians in revealing the etiology of rotator cuff degeneration and determining the surgical method to be used for treatment.

NCT ID: NCT05721560 Active, not recruiting - Clinical trials for Rotator Cuff Tears (RCTs)

SINEFIX-2022 Pilot Phase

Start date: September 12, 2023
Phase: N/A
Study type: Interventional

Shoulder pain is one of the most commonly reported musculoskeletal complaints, which negatively affects upper limb use, night rest, daily life activities, work, sports performance and autonomy. Rotator cuff disease represents the most common cause of shoulder pain and it is responsible for up to 70% of all shoulder related visits to clinicians. Its incidence furthermore is expected to grow as the population ages. A wide range of conditions are included under the umbrella term of rotator cuff disease, including rotator cuff tendinopathy, subacromial bursal pathology, and partial-thickness or full-thickness rotator cuff tears (RCTs). The latter ones, i.e. rotator cuff tears, form the indications for which the test devices, the SINEFIX implant and instruments, are intended. Despite the high prevalence of this condition, the pathophysiology and healing potential are not well understood, making the condition challenging to predictably treat in some patient populations. RCTs may occur in young people as a consequence of trauma (e.g. acute shoulder dislocation), however RCTs typically present in middle-aged or elderly people and cannot always be attributed to precipitating events or trauma. Instead, they can be attributed to degenerative processes, and are therefore referred to as degenerative RCTs. For RCTs, treatment options include both surgical and non-surgical (conservative) procedures. In this context, the SINEFIX implant and instruments were developed to treat adult patients with rotator cuff lesions of size up to 2 cm through arthroscopic reconstruction.

NCT ID: NCT05721547 Completed - Rotator Cuff Tears Clinical Trials

Alterations in Spinal Alignment and Mobility in Individuals With Arthroscopic Rotator Cuff Repair

Start date: June 20, 2018
Phase:
Study type: Observational [Patient Registry]

The aim of this observational study was to the alterations in spinal alignment in individuals who have undergone RC surgery and revealed the differences compared to healthy individuals.

NCT ID: NCT05720286 Completed - Clinical trials for Rotator Cuff Injuries

Performance and Safety of the FIXIT® Anchor in Arthroscopic Rotator Cuff Repair

FIXIT®2018
Start date: December 12, 2018
Phase:
Study type: Observational

Verification of the performance and safety of the first row resorbable threaded anchor FIXIT® in arthroscopic rotator cuff repair Non-interventional, prospective, non-comparative, multi-center study as part of the post-marketing follow-up of devices

NCT ID: NCT05695820 Recruiting - Clinical trials for Shoulder Impingement Syndrome

Effects of Low- Load Strengthening Using Different Exercises Modes During Blood Flow Restriction for Treating Shoulder Impingement Syndrome

Start date: February 13, 2023
Phase: N/A
Study type: Interventional

Purpose of the study: This study compares effects of isometric, concentric and eccentric exercises for shoulder muscles by using low load blood flow restriction training on pain, strength and function in patients with SIS.

NCT ID: NCT05690776 Recruiting - Rotator Cuff Tears Clinical Trials

PMCF Study on the Safety, Performance and Clinical Benefits Data of the Quattro X Broadband

Start date: June 17, 2022
Phase:
Study type: Observational

The study is a multicenter, retrospective and prospective, non-randomized, noncontrolled, and consecutive series post-market study. The purpose of this study is collect data confirming safety, performance and clinical benefits of the Quattro® X Suture Anchor with BroadBand™ Tape and Instruments when used in rotator cuff repair. The primary endpoint of this study is the assessment of performance by analyzing soft tissue to bone healing in the shoulder (rotator cuff). Healing will be assessed by the investigator using PROMs and clinical outcomes of the patient. The clinical benefit will be assessed by functional outcomes measured using standard and well-established scoring systems (e.g. Constant & Murley and EQ-5D-5L) at 1 year post-operative. The safety will be assessed by monitoring the incidence and frequency of device- and/or procedure-related adverse events.

NCT ID: NCT05670080 Not yet recruiting - Shoulder Pain Clinical Trials

Does MI Have a Therapeutic Role in Arthroscopic Rotator Cuff Repair?

Start date: September 15, 2025
Phase: N/A
Study type: Interventional

Objective: The aim of this study is to investigate the effect of motor imagery on muscle activity, pain, and function in arthroscopic rotator cuff repair. Methods: As a result of the power analysis (G-Power), 36 participants are planned to be included in this study Block randomization will be used to divide participants into 2 groups, each with at least 18 participants: Group 1 (MI group) and Group 2 (Control group) (Randomizer.org). Both groups will receive a 4-week physical therapy program. MI (Motor Imagination) group will receive a motor imagination program in addition to the physical therapy program. Data will collect using the visual analog scale (VAS), goniometric measurement, circumference measurement, Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH), Kinesthetic and Visual Imagery Questionnaire- KVIQ-20, Tampa Kinesiophobia Scale, 3-question satisfaction questionnaire, superficial Electromyography (EMG) (BTS Bioengineering Free EMG 100 RT). Practice Implications: The current study will contribute to understanding how motor imagination affects muscle activity and muscle atrophy.