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Bursitis clinical trials

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NCT ID: NCT01506154 Completed - Shoulder Pain Clinical Trials

Safety & Efficacy Study of MRX-7EAT Patch in the Treatment of Pain of the Shoulder

Start date: December 2011
Phase: Phase 3
Study type: Interventional

A Randomized, Multi-Center, Double-Blind, Placebo-Controlled Phase III Trial to Evaluate the Efficacy, Tolerability and Safety of MRX-7EAT Etodolac-Lidocaine Topical Patch in the Treatment of Pain due to Recent Onset Supraspinatous and/or Subacromial Tendonitis/Bursitis and/or Subdeltoid Bursitis of the Shoulder.

NCT ID: NCT01483963 Completed - Adhesive Capsulitis Clinical Trials

AA4500 for the Treatment of Adhesive Capsulitis of the Shoulder

Start date: November 2011
Phase: Phase 2
Study type: Interventional

The objectives of this study are to assess the safety, effectiveness, and immunogenicity of AA4500 in the treatment of adhesive capsulitis.

NCT ID: NCT01458691 Completed - Adhesive Capsulitis Clinical Trials

Intra-articular Injection of Allogeneic Platelet Rich Plasma (PRP) for Adhesive Capsulitis

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of intra-articular allogenic Platelet Rich Plasma injection and steroid injection in the treatment of adhesive capsulitis of the shoulder.

NCT ID: NCT01406652 Completed - Patellar Bursitis Clinical Trials

Optimisation of the Treatment of Infectious Bursitis

Start date: May 2011
Phase: N/A
Study type: Interventional

The study investigates prospectively the cost-savings related to a one-stage bursectomy (debridement, drainage and closure at the same time) versus two-stage bursectomy (debridement, left open and closure at a second time) of severe bursitis among hospitalized patients for surgical treatment of septic bursitis. We suppose that the one-stage bursectomy reveals similar recurrence rates but is associated with a significant shortening of hospital stay, consumption of resources and increased patient satisfaction.

NCT ID: NCT01306708 Completed - Adhesive Capsulitis Clinical Trials

Amitriptyline Regarding Nimesulide in Acute Idiopathic Adhesive Capsulitis

Start date: February 2011
Phase: Phase 2
Study type: Interventional

The adhesive capsulitis is a disease of the shoulder characterized by pain and limitation of movement amplitude. It is defined as for etiology, having discordant theories that related it to an inflammatory condition or to an algoneurodystrophy process. There is not yet a consensus about the best option of treatment. The non-steroidal anti-inflammatories have analgesic and anti-inflammatory activity, where the mechanism of action is the inhibition of prostaglandin synthesis. The antidepressants have been increasingly used in the control of chronic pain and the major action mechanism to have the analgesic effect seems to be based on inhibition of neurotransmitters reuptake noradrenaline and/or serotonin) in nerve cell endings. Literature studies associate the practice of the nerve suprascapular blockade with anaesthetics to good results of clinical improvement of the pain, however, so far, no clinical studies comparing the efficacy of the non-steroidal antiinflammatories or tricyclic antidepressants to nervous blockage were registered in the acute treatment of adhesive capsulitis.

NCT ID: NCT01205477 Completed - Bursitis Clinical Trials

Safety and Efficacy of Methylprednisolone Infiltration in Anserine Bursitis Treatment

Start date: September 2009
Phase: Phase 2
Study type: Interventional

To investigate the safety and efficacy of methylprednisolone infiltration in anserine bursitis treatment

NCT ID: NCT01161615 Completed - Bursitis Clinical Trials

MRX-7EAT Etodolac-Lidocaine Topical Patch in the Treatment of Tendonitis and Bursitis of the Shoulder

Start date: July 2010
Phase: Phase 3
Study type: Interventional

A Randomized, Multi-Center, Double-Blind, Placebo-Controlled Phase III Trial to Evaluate the Efficacy, Tolerability and Safety of MRX-7EAT Etodolac-Lidocaine Topical Patch in the Treatment of Tendonitis and Bursitis of the Shoulder.

NCT ID: NCT01157221 Completed - Frozen Shoulder Clinical Trials

Prediction Frozen Shoulder Validation

Start date: August 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Background: Few studies have examined the predictors of the clinical course of subjects with frozen shoulder syndrome or explained the persistence of symptoms after appropriate therapy. Altered shoulder kinematics may predispose subjects to subacromial impingement, rotator cuff tendonitis, altered shoulder joint forces, and possible degenerative changes. Subsequently, a more difficult and chronic course of frozen shoulder syndrome may develop. Objective: The purposes of this study are: (1) to develop a prediction method for determining altered shoulder kinematics and associated muscular activities which are associated with the chronicity of frozen shoulder dysfunction, and (2) to validate this prediction method and analyze the impact of the method on clinical behavior. Design: For the first year, a prospective study will be conducted to develop a prediction method that will identify impaired shoulder kinematics associated with the degree of symptom-related functional disability in patients with frozen shoulder syndrome. For the second and third years, validation of the proposed prediction method will determine whether altered shoulder kinematics and associated muscular activities subject to intervention meet the prediction criteria and demonstrate improvement in their follow-up, which will be shown to improve decision making in clinical practice.

NCT ID: NCT01144533 Completed - Adhesive Capsulitis Clinical Trials

Comparative Analysis of Intra-articular Injection of Steroid and/or Sodium Hyaluronate in Adhesive Capsulitis

Start date: June 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of intra-articular steroid injection, sodium hyaluronate injection, a combination of the two, and placebo in the treatment of adhesive capsulitis of the shoulder.

NCT ID: NCT01087229 Completed - Adhesive Capsulitis Clinical Trials

Effectiveness of an Oxygen-nitrous Oxide Mixture During Physical Therapy for Frozen Shoulder

MEOPA
Start date: March 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether or not the use of an equimolar mixture of oxygen and nitrous oxide during the physical therapy for patients suffering from frozen shoulder (adhesive shoulder capsulitis) results in a gain in shoulder amplitude (Constant Score) and less pain as compared to patients undergoing physical therapy without this treatment.