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Shoulder Pain clinical trials

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NCT ID: NCT00743600 Completed - Shoulder Pain Clinical Trials

Ultrasound Evaluation of the Rotator Cable and Associated Structures.

Start date: September 2005
Phase: N/A
Study type: Interventional

This study will use healthy volunteers and patients with shoulder problems (pain or impaired movement). Ultrasound will be used to image and document the appearance of both normal and abnormal shoulder structures.

NCT ID: NCT00732589 Completed - Stroke Clinical Trials

SSNB in Hemiplegic Shoulder Pain

SSNB
Start date: August 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare suprascapular nerve block with therapeutic ultrasound in stroke patients who have shoulder pain in weak side.

NCT ID: NCT00703729 Completed - Postoperative Pain Clinical Trials

Compression and Cold Therapy on the Post-Operative Shoulder

Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate and compare clinical post-operative outcomes for patients using active cooling and compression device and those using ice bags and elastic wrap after acromioplasty or arthroscopic rotator cuff repair.

NCT ID: NCT00680537 Completed - Shoulder Pain Clinical Trials

Physical Therapy Program for Prevention of Shoulder Pain After Device Implant

Start date: April 2008
Phase: N/A
Study type: Interventional

This is a clinical research study to determine if a prescribed physical therapy intervention after subcutaneous implantation of an implanted cardioverter-defibrillator (ICD) or pacemaker reduces the incidence of rotator cuff tendonitis when compared to usual post procedural care.

NCT ID: NCT00680472 Completed - Pain Clinical Trials

HKT-500 in Adult Patients With Shoulder Pain

Pain
Start date: April 2008
Phase: Phase 3
Study type: Interventional

The objective of this study is to determine the efficacy of HKT-500 in subjects with acute shoulder pain

NCT ID: NCT00679887 Completed - Shoulder Pain Clinical Trials

Chronic Shoulder Pain Treated by Pressures With the Thumbs on the Trigger Points

Start date: September 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find the efficacy of treating the trigger points located around the shoulder in patients suffering from chronic shoulder pain.

NCT ID: NCT00661089 Completed - Clinical trials for Post-stroke Shoulder Pain and Spasticity

Randomized DB Controlled Trial of Botulinum Toxin A in Hemiplegic Shoulder Pain and Spasticity

Start date: September 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether botulinum toxin type A injected into muscles around the shoulder is effective in treating shoulder pain and improving function in patients with shoulder pain and involuntary muscle tightness after a stroke.

NCT ID: NCT00634608 Completed - Obesity Clinical Trials

Integrating Targeted MedlinePlus Health Prescriptions Into Clinic Practice Workflow

Start date: February 2008
Phase: N/A
Study type: Interventional

The specific aim of this proposed project is to implement a standard process for integrating MedlinePlus health information prescriptions into the clinic workflow. Hypothesis 1: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more likely to seek information / use MedlinePlus compared with individuals in the control group. Hypothesis 2: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more satisfied with the information received compared with individuals in the control group.

NCT ID: NCT00597766 Completed - Shoulder Pain Clinical Trials

Subacromial Corticosteroid Injection for Hemiplegic Shoulder Pain

Start date: December 2007
Phase: Phase 2
Study type: Interventional

This is a double-blinded study of subacromial corticosteroid injection (steroid injection to the shoulder) to treat shoulder pain in the paralyzed (hemiplegic) shoulder of chronic stroke survivors. This study is designed to evaluate pain relief of a standard steroid injection treatment, compared to a high dose treatment and a low dose treatment, for shoulder pain in stroke survivors. A total of 105 chronic stroke survivors with moderate to severe shoulder pain will be enrolled. All eligible participants will undergo an initial test injection to localize pain to the subacromial space. If this turns out to be positive, the subjects will be randomly assigned to one of three groups: 1. low dose group which receives 20mg of steroid (triamcinolone) injection to the subacromial space of the affected shoulder; 2. standard dose group which receives a standard 40mg of steroid (triamcinolone) injection to the subacromial space of the affected shoulder; or 3. high dose group which receives 60mg of steroid (triamcinolone) injection to the subacromial space of the affected shoulder. Study participants will all rate their pain in interviews (Baseline, weeks 1, 2, 3, 4, 8, 12 (7 times) and in laboratory-based measures that will be administered at baseline, weeks 4, 8, 12 (4 times). Subjects will be followed for a total of 13 weeks. The study will thus characterize the dose response of triamcinolone for the treatment of hemiplegic shoulder pain.

NCT ID: NCT00587626 Completed - Neck Pain Clinical Trials

Proposal to Evaluate the Efficacy of the InterX 5000 in the Treatment of Chronic Neck and Shoulder Pain

Start date: August 2007
Phase: Phase 2
Study type: Interventional

The purpose of the proposed study is to evaluate the efficacy of the InterX 5000 in relieving chronic neck and shoulder pain. This study will focus on the efficacy of treating patients who have functional limitations in activity because of chronic/recurrent neck or shoulder pain. H1: InterX therapy will have a moderate effect to reduce pain. H2: Functional gains will be greater in patients receiving InterX therapy compared to those who received placebo treatment. H3: Chronic neck and shoulder pain is more prevalent in patients who exhibit radiographic evidence of degenerative spondylosis/arthrosis of the cervical spine.