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Rotator Cuff Injuries clinical trials

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NCT ID: NCT02679352 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

SMR Stemless Shoulder Arthroplasty Clinical Study

Start date: March 2016
Phase: N/A
Study type: Interventional

Shoulder arthroplasty is a reliable procedure for the treatment of severe shoulder joint diseases to relieve pain and restore shoulder function. Shoulder implants commonly used are characterised by a humeral stem and complications related to the stem are not infrequent. These include: bone stock loss, intraoperative and postoperative break around the implant, malpositioning of the humeral component and difficult eradication of infections inside the bone around the implant. With the aim of reducing stem-related complications, a novel prosthesis characterised by a stem-less design has been developed. The objective of this study is therefore to explore how well people recover after shoulder replacement with this novel stem-less shoulder prosthesis. This will be assessed over 5 years in three different countries in Europe using patient completed questionnaires and clinical and radiographic assessments.

NCT ID: NCT02670174 Completed - Clinical trials for Shoulder Impingement Syndrome

Influence of Kinetic Chain Training on the Treatment Outcome of Overhead Athletes With Impingement

Start date: September 2015
Phase: N/A
Study type: Interventional

A randomized controlled trial will be conducted to examine the effectiveness of a traditional home exercise program versus 2 kinetic chain home exercise programs on treatment outcome of overhead athletes with shoulder impingement syndrome. Primary outcome measures are reduction of pain and disability, and improvement in functionality and sports performance. Secondary outcome measures are strength, mobility, flexibility and functional performance.

NCT ID: NCT02644564 Completed - Rotator Cuff Tear Clinical Trials

Early Clinical Examination and Ultrasonography Screening of Acute Soft Tissue Shoulder Injuries

Start date: October 5, 2015
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the introduction of early ultrasonography screening will change the diagnostic spectrum of soft tissue shoulder injuries in patients aged forty years or more. We also want to study whether certain physical tests will be able to predict or rule out full-thickness tears of the rotator cuff (shoulder tendons) in the acute phase. Another purpose is to explore the course of soft tissue shoulder injuries over a year, as well as to compare the results to studies on the prevalence of rotator cuff full-thickness tears.

NCT ID: NCT02643017 Completed - Rotator Cuff Tear Clinical Trials

Effect of Dexmedetomidine on Postoperative Cognitive Function in Patients Undergoing Shoulder Arthroscopy With Beach Chair Position Under Desflurane Anesthesia

Start date: December 11, 2015
Phase: N/A
Study type: Interventional

Investigate the effects of dexmedetomidine on postoperative cognitive function in patients undergoing shoulder arthroscopy with beach chair position under desflurane anesthesia.

NCT ID: NCT02631486 Completed - Rehabilitation Clinical Trials

Does Early Mobilisation Improve Outcomes After Rotator Cuff Repair?

Start date: April 2016
Phase: N/A
Study type: Interventional

Shoulder pain is among the most common musculoskeletal complaints, leading to high number of General Practioners consultations in the United Kingdom. On the top list of the disorders causing pain and dysfunction of shoulder is rotator cuff tears. The aetiology of rotator cuff tears is multifactorial and is likely to be a combination of age-related degenerative changes and trauma during life. It is present in approximately 25% of individuals in their 60s and 50% of individuals in their 80s and have been shown to start developing during the 40s. To recover functional status of this patients group, surgical repair is often recommended, but for optimal results the rehabilitation is of great importance and must be adequately planned. After surgery a period of movement restriction is followed, however, the optimal time of immobilisation is unknown. As a common practice, patients use a sling for six weeks and avoid any activities with the affected shoulder. This period is important to protect the tendon, allow good healing and to possibly prevent re-tear episodes. Although, the delayed motion may increase the risk of postoperative shoulder stiffness, muscle atrophy and potentially delay improvement of functionality. Based on the available evidence, it is difficult to make a clinical decision for a well-programmed rehabilitation regime and establish the most favourable postoperative time to start it. Moreover, it is not clear if early mobilisation will benefit more severe stages as published studies have methodological flaws that compromises the clinical decision for patients with higher commitments. The question whether early mobilisation application is beneficial is of high importance as the results will not just help improving patients quality of life, but also may reduce costs as further complication may be avoided.

NCT ID: NCT02588027 Active, not recruiting - Clinical trials for Rotator Cuff Tear Arthropathy

Effect of Ibuprofen on Postoperative Opiate Medication Use and Shoulder

Start date: October 2015
Phase: N/A
Study type: Interventional

This will be a randomized controlled trial to determine if postoperative ibuprofen after arthroscopic rotator cuff repair impacts postoperative opiate medication use, Visual Analog Scale (VAS) pain scores, shoulder range of motion (ROM), and repair integrity.

NCT ID: NCT02528084 Completed - Clinical trials for Rotator Cuff Injuries

The Effects of Yoga on Patients With Rotator Cuff Injuries

Start date: October 20, 2015
Phase: N/A
Study type: Interventional

To determine if patients who undergo a 6-week online yoga exercise treatment differ from those who undergo a 6-week online standard exercise intervention and patients who do not undergo any treatment (the control).

NCT ID: NCT02512536 Completed - Clinical trials for Rotator Cuff Tear Arthropathy

Does Botulinum A Toxin Help With Pain From Rotator Cuff Arthropathy?

Start date: July 2016
Phase: Phase 2
Study type: Interventional

Rotator cuff arthropathy is a cause of shoulder arthritis which is a common condition seen both in primary and secondary care. It is a painful condition, with significant disability. Specialist shoulder replacements have found acceptance within the trust, nationally and internationally although there are high complication rates. There is however a significant cost difference (fifty fold) between a reverse total shoulder replacement and a botox injection, and to date there have been no randomised control trials, or any registered, comparing the use of a botox injection for pain relief in cuff arthropathy versus no treatment. If there is a significant clinical difference in the pain outcomes between the two, this could result in significant savings to the NHS and the taxpayer as a whole. If high levels of pain relief could be predictably obtained using Botulinum A toxin injections then potentially patients could avoid the need for surgery.

NCT ID: NCT02495818 Completed - Clinical trials for Rotator Cuff Syndrome

Suprascapular Nerve Block Guided by Ultrasound

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of suprascapular nerve block guided by ultrasound combined with home exercises compared with placebo. Pain intensity, function, pressure pain threshold and goniometry were designed to be assessed in all patients.

NCT ID: NCT02493660 Completed - Clinical trials for Rotator Cuff Syndrome

A Pivotal Study to Assess the InSpaceā„¢ Device for Treatment of Full Thickness Massive Rotator Cuff Tears

Start date: June 26, 2015
Phase: N/A
Study type: Interventional

A pivotal study to assess the safety and effectiveness of the InSpaceā„¢ device implantation in comparison to surgical partial repair of full thickness Massive Rotator Cuff Tear (MRCT).