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Shoulder Pain clinical trials

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NCT ID: NCT03592056 Terminated - Postoperative Pain Clinical Trials

Hemidiaphragmatic Paralysis With Diluted Continuous Interscalene Plexus Infusions

Start date: August 10, 2018
Phase:
Study type: Observational [Patient Registry]

Interscalene brachial plexus block (ISB) constitutes the analgesic criterion standard for shoulder surgery. However, it is associated with a high incidence of hemidiaphragmatic paralysis (HDP) that may not be tolerated by patients with chronic pulmonary disease. Continuous ISBs have not avoided this complication with the reported and regularly used local anesthetic dilutions (i.e. 0.125% bupivacaine, 0.25% ropivacaine, etc). This observational study will register the incidence of HDP in continuous interscalene block (CISB) using a very diluted solution of levobupivacaine (0.04%) in patients undergoing arthroscopic shoulder surgery. The main objective of this study is to determine the frequency of HDP the first postoperative day before patient discharge(POD).

NCT ID: NCT03588143 Completed - Clinical trials for Shoulder Pain Chronic

Immediate Effects of TENS and HVPS on Subacromial Pain and Shoulder Movements

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

This study was performed to investigate the immediate effects of transcutaneous electrical nerve stimulation (TENS) and high voltage pulsed stimulation (HVPS) on resting pain and pain-free range of shoulder motion (pfROM) in patients with subacromial pain syndrome (SAPS).

NCT ID: NCT03586934 Withdrawn - Opioid Use Clinical Trials

Multimodal Analgesia in Shoulder Arthroplasty

Start date: June 1, 2018
Phase: Phase 3
Study type: Interventional

Opioid medications are associated with many side effects and the risk of abuse or overdose. Orthopaedic surgeons are currently investigating ways to control pain after surgery while limiting the amount of opioid medications prescribed. One way to reduce the amount of opioid medications prescribed, and potentially avoid opioid-associated adverse events, is to use multiple non-opioid medications and anesthetic drugs before surgery, during surgery, and after surgery. This study aims to evaluate a protocol with non-opioid pain medications to reduce the need for opioid medication after shoulder surgery.

NCT ID: NCT03586154 Completed - Breast Neoplasms Clinical Trials

Combined Intra-articular Shoulder Injection and Stellate Ganglion Block in Chronic Post-mastectomy Shoulder Pain

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

Background and Purpose: Adhesive capsulitis of the shoulder is commonly found in patients after breast cancer treatment. We aimed to determine the effectiveness of combined shoulder joint intra-articular injection of platelet rich plasma (PRP) with stellate ganglion block (SGB) with ketamine &bupivacaine injection as a new technique for frozen shoulder (FS) management after mastectomy. Methods: Sixty four patients with chronic post-mastectomy shoulder pain and stiffness were randomly allocated into one of two groups: group A; ultrasound guided SGB (1 ml ketamine in a dose of 0.5mg/kg plus 5ml bupivacaine 0.5% in total volume 10 ml) and group B; ultrasound guided SGB plus posterior approach shoulder injection with PRP. Visual analogue score (VAS) at rest and at shoulder movement, range of motions (ROM) of shoulder and disability of arm, shoulder and hand (DASH) questionnaire were recorded.

NCT ID: NCT03554538 Not yet recruiting - Clinical trials for Shoulder Impingement Syndrome

Efficacy of a Web App With Multimedia Animations to Teach Therapeutic Exercise in Shoulder Pain

Start date: November 2019
Phase: N/A
Study type: Interventional

The aim of this trial is to develop and evaluate a web app to teach patients about how to correctly perform a tailored program of shoulder exercises. The exercise program will be evidence based, and there will be two groups in the study, both exercising. The follow up will be of 6 months.

NCT ID: NCT03547570 Completed - Clinical trials for Shoulder Pain Chronic

Resistance Training for Patients With Hypermobility Spectrum Disorders and Shoulder Symptoms: a Feasibility Study

Start date: May 4, 2018
Phase: N/A
Study type: Interventional

Hypermobility Spectrum Disorders (HSD) is a recent diagnosis that covers joint hypermobility with one or more secondary symptomatic musculoskeletal manifestations. Current clinical management of this population with shoulder symptoms is a non-standardized combination of physiotherapy modalities including exercise prescription. There is evidence suggesting that progressive heavy resistance training increases muscle strength and tendon stiffness, which may be valuable for treatment of this population. The aim of this study is to evaluate the feasibility of progressive heavy shoulder resistance training (PHSRT) for adults with HSD and shoulder symptoms.

NCT ID: NCT03546777 Completed - Shoulder Pain Clinical Trials

Evaluation Coroacromial Ligament Thickness

Start date: March 1, 2017
Phase:
Study type: Observational

In this study, it was aimed to determine the relationship between pathologic findings and coracoacromial ligament thickness in magnetic resonance imaging in shoulder pain patients.

NCT ID: NCT03528499 Completed - Shoulder Pain Clinical Trials

Scapular Movement Training Versus General Exercises for Individuals With Shoulder Pain

Start date: August 21, 2018
Phase: N/A
Study type: Interventional

Interventions focused on the scapula have been frequently used to treat shoulder pain. However, most studies do not assess the contribution of scapular movement alteration for the symptoms. Objectives: To compare the effects of two interventions for shoulder pain: Scapular Movement Training and General Exercises.

NCT ID: NCT03523884 Not yet recruiting - Shoulder Pain Clinical Trials

Effectiveness of Technology-enabled Exercise Program in Firefighters With Shoulder Pain.

Start date: June 2018
Phase: N/A
Study type: Interventional

To assess if a technology-enabled Exercise program plus Education (TEEP + E) is more effective than Education program (EP) alone, in providing better outcomes (quality of life, at-work disability and productivity loss, firefighters' perception, adherence, overall improvement/deterioration) in firefighters with shoulder pain, at 3-, 6-and 12-month follow ups.

NCT ID: NCT03521856 Completed - Shoulder Pain Clinical Trials

Trial for Shoulder Pathology and Pain in Chronic SCI

Start date: May 2, 2012
Phase: N/A
Study type: Interventional

This research study will investigate in a 12-week home exercise program to see whether it is effective in improving shoulder pathology and reducing shoulder pain in persons with chronic spinal cord injury. The research study will involve ultrasound shoulder examinations of your shoulders using a non-invasive medical ultrasound machine, as well as clinical shoulder examinations and completion of a number of pain questionnaires.