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Bursitis Clinical Trials

A listing of Bursitis medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (34) clinical trials

Recover L-PRP in Lateral Epicondylitis (REGP-11-00)

Clinical trials have been conducted to determine the efficacy and safety of Leukocyte- and Platelet-Rich Plasma (L-PRP) prepared with Biomet Recover L-PRP Mini Platelet Separation Kit for the treatment of tendinosis in a controlled setting. This study will allow for the capture and evaluation of real-world clinical data on a ...

Phase N/A

Impact of Platelet Rich Plasma Over Alternative Therapies in Patients With Lateral Epicondylitis

Platelet rich plasma (PRP) deserves study because it is more expensive than the other treatments. If we learn that PRP is better compared to the other treatments, it would justify the high cost and growing industry associated with the procedure. If we find out that PRP is not better compared ...

Phase

Comparison Between Type A Botulinum Toxin Injection and Corticosteroid Injection in the Treatment of Tennis Elbow

Humeral lateral epicondylitis or tennis elbow is a common painful elbow disorder. The cause of tennis elbow is the chronic overload of bone-tendon junction. High prevalence of tennis elbow has a direct impact on the workplace productivity and quality of life. Steroid injection is the very few methods proved to ...

Phase N/A

Mobilization Techniques in Patients With Frozen Shoulder: a Randomized Multiple-Treatment Trial

We will carry out a multiple-treatment trial on two groups. The multiple-treatment trial involves the application of two or more treatments in one single-subject [Portney and Watkins, 2000; Barlow and Hersen, 1984]. It is used to compare the effects of two or more treatments. Consenting patients will be randomized by ...

Phase N/A

Hydrothermal Ablation in Recurrent and Chronic Symptomatic Bursitis

This is an open, exploratory, 6-months dose-tolerance and dose-response study of a single thermal ablation (Ablaflex) procedure in subjects suffering from chronic symptomatic bursitis. Possible study participants will be screened for eligibility based on defined inclusion and exclusion criteria. Eligible patients will be administered with a single 3-minute perfusion of ...

Phase N/A

Spray vs EMLA Cream on Pain During Intra-articular Injection

All participants are randomly allocated to the spray group, EMLA group and placebo group. In spray group, participants receive an application of placebo cream at the needle electrode insertion site 60 minutes before needle insertion, and a self adhering dressing is placed over the site. After 60 minutes, the dressing ...

Phase

Dry Needling Manipulation and Stretching vs. Manual Therapy Exercise and Ultrasound for Lateral Epicondylalgia

Patients with epicondyalgia will be randomized to receive 2 treatment sessions per week for 4 weeks (up to 8 sessions total) of either: (1) electric dry needling, thrust manipulation and stretching or (2) impairment-based manual therapy, exercise and ultrasound

Phase N/A

Manipulation Under Anesthesia Versus Arthroscopic Capsular Release in the Treatment of Adhesive Capsulitis

Shoulder pain is one of the most common causes of musculoskeletal disability in the adult population. Adhesive capsulitis is one of a multitude of pathologic entities that can cause shoulder pain and dysfunction. The condition is seen frequently in the clinics of primary care providers and orthopedic surgeons. Patients who ...

Phase N/A

Adhesive Capsulitis: Prospective Analysis of Efficacy and Financial Impact for Use of Physical Therapy in Treatment

Objectives The purpose of this study is to identify individuals 18 or older who have diagnostic presentation of adhesive capsulitis and randomize them into two arms, distinguished by use of physical therapy and steroid injections compared with steroid injections followed by watchful waiting. This prospective study will be used to ...

Phase

Effect of Ultrasound-guided Suprascapular Nerve Block Versus Intra-articular Corticosteroid Injection for Frozen Shoulder

The inclusion criteria is: 1. unilateral side involvement; 2. 50% loss of passive ROM (external rotation or abduction) in the glenohumeral joint comparing to the unaffected side; 3. duration of symptoms 3 months. 4. age 20year old. The exclusion criteria include: 1. ever received manipulation of the affected shoulder with/without ...

Phase N/A