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Rotator Cuff Tendinosis clinical trials

View clinical trials related to Rotator Cuff Tendinosis.

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NCT ID: NCT04985370 Suspended - Clinical trials for Rotator Cuff Tendinosis

PNE Plus Exercise Versus Exercise for Chronic Rotator Cuff Tendinopathy

Start date: July 25, 2021
Phase: N/A
Study type: Interventional

The aim of this randomized controlled trial is to evaluate the combined effects of pain neuroscience education plus exercise to exercise alone in the management of patients with chronic rotator cuff tendinopathy regarding pain, function, strength, kinesiophobia, and pain catastrophizing.

NCT ID: NCT04923477 Recruiting - Clinical trials for Rotator Cuff Injuries

Therapeutic Exercise for Rotator Cuff Tendinopathy / Subacromial Pain Syndrome - Outcomes and Mechanisms

Start date: June 8, 2021
Phase: N/A
Study type: Interventional

Rotator cuff tendinopathy, one of the pathologies identified as part of the cluster of shoulder symptoms known as subacromial pain syndrome, is a common musculoskeletal shoulder condition. Resolution of pain and disability is poor despite treatment, with only about 50% reporting full recovery at 12 - 18 months. Prior studies suggest therapeutic exercise when used alone and with other interventions can have positive outcomes; however, not all patients with rotator cuff tendinopathy respond. Few studies have assessed the effects of exercise for individuals with chronic pain, especially brain driven mechanisms, thought to play a key role. In this study, we will use brain imaging to understand the mechanisms, identify predictors of a positive response to exercise, and the relationship to biomechanical and pain-related factors in patients with RC tendinopathy. The findings from this study will optimize the delivery and treatment response to exercise for individuals with shoulder pain.

NCT ID: NCT04806191 Recruiting - Shoulder Pain Clinical Trials

Simple and Evidence-based Examination and Treatment of Shoulder Pain in General Practice

EASIER
Start date: March 11, 2021
Phase: N/A
Study type: Interventional

Previous research suggests that general practitioners find handling patients with shoulder pain difficult and that the current care for shoulder pain is not in line with the best available evidence (1).This project aims to assess the effectiveness, costs and implementation of an evidence-based guideline for shoulder pain in general practice.

NCT ID: NCT04640662 Completed - PRP Clinical Trials

The Effects of Platelet-Rich Plasma Versus Prolotherapy On Rotator Cuff Tendinopathy: A Randomized Controlled Trial.

Start date: February 17, 2020
Phase: Phase 1
Study type: Interventional

Rotator cuff tendinopathy is the common cause of shoulder pain in the working-age group and the elderly (1). The condition reported takes an average of 10 months or longer to recover. Treatment ranges from non-surgical therapy through exercise, physiotherapy, injections to surgery (2). Injection of steroid was used in many cases to reduce pain. However, steroid only provided short term pain relief and did not resolve the main pathology. Emerging of biologics agents such as platelet-rich plasma (PRP) and prolotherapy are alternative to the treatment (3). PRP is a concentrated platelet which contains a high concentration of protein that helps in the healing process (4). Prolotherapy with the commonly used substance dextrose works by attracting inflammatory substrate and stimulate own body healing process (5). This study takes place at the University of Malaya Medical Centre. Participants diagnosed with rotator cuff tendinopathy are randomly divided into two groups- Platelet Rich Plasma (PRP) group and Prolotherapy group. All participants are screened by the researcher for the eligibility to join the study. Subsequently, the participants undergo baseline assessment on the clinical, functional, biomechanics and ultrasound. Blood is taken in all patient, to make the patient blind to the intervention they received. In the PRP group- the participants received 2ml of PRP, and in prolotherapy group, the participants received 2ml of 16.5% dextrose solution. A single injection is done by an experienced Sports Physician using ultrasound-guided into the injured area. The assessor at baseline, and follow up are blinded to the intervention. The participants need to come for follow up at 3 weeks, 6 weeks, 3 months and 6 months after injection. Systematic reviews showed the benefit of biologics agent to treat tendon injuries, especially for lateral epicondylitis and patellar tendinitis (6). Many studies for soft tissue injury were on PRP compared to prolotherapy. This study hypothesized that both treatments result in significant improvement in pain and function after the intervention. PRP might provide more significant improvement compared to prolotherapy.

NCT ID: NCT04502134 Recruiting - Rotator Cuff Tears Clinical Trials

Association Between Tendon-related Transcription Factor and Ultrasound Images and Shoulder Function

Start date: November 30, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this project is to extract effusions and damaged tendons during tendon repair therapy in patients with tendon tears. Then, we would analyze tendon-related transcription factors from histology and cytology, and compare changes in tendon with ultrasound images. Helps to understand the mechanism of tendon lesions.

NCT ID: NCT04492748 Active, not recruiting - Rotator Cuff Tears Clinical Trials

Rotator Cuff Tendinopathy Conservative Treatment With Collagen, PRP or Both

RCCT
Start date: July 1, 2020
Phase: Phase 4
Study type: Interventional

The aim of the trial is comparison of the effectiveness of three methods of conservative treatment in partial thickness rotator cuff injury (PTRCI): collagen with PRP injections, PRP injections alone and collagen injections alone.

NCT ID: NCT04333784 Completed - Clinical trials for Rotator Cuff Tendinosis

Blood Flow Restriction Training in Patients With Shoulder Pain

Start date: December 21, 2020
Phase:
Study type: Observational

This study was planned to investigate the effect of blood flow restriction exercise training on shoulder muscle strength and muscle thickness, and to determine the change in pain and symptoms in patients with rotator cuff tendinopathy. Patients in the study group will perform the rehabilitation exercises with a pneumatic cuff and blood flow restricted. The patients in the control group will perform the same exercise program without restricting blood flow.

NCT ID: NCT03967574 Completed - Clinical trials for Rotator Cuff Injuries

Subacromial Corticosteroid Injections and tDCS in Rotator Cuff Tendinopathy

Start date: November 4, 2015
Phase: N/A
Study type: Interventional

This study evaluates the effects of corticosteroid injections over time, as well as the additional effect provided by subsequent transcranial direct current stimulation (tDCS) of the motor cortex on patients with rotator cuff tendinopathy of the shoulder. All patients will receive a subacromial corticosteroid injection. Two weeks later, a third will receive a treatment of tDCS, a third will receive a placebo a-tDCS treatment, and the last third will not receive any additional treatment.