Clinical Trials Logo

Epicondylitis clinical trials

View clinical trials related to Epicondylitis.

Filter by:
  • Completed  
  • Page 1

NCT ID: NCT04729400 Completed - Epicondylitis Clinical Trials

Percutaneous Electrolysis and Vacuum Myofascial Therapy deviceTrial.

Start date: June 10, 2021
Phase: N/A
Study type: Interventional

The concept of epicondylitis refers to the manifestation of pain in the area of insertion of the epicondile muscles, and that it is accompanied by limitation functional. A tendinopathy is characterized as a process of degeneration, with fibroblast proliferation and disorganization of the fibers of collagen. This tendon pathology especially affects the epicondyle extensors and especially the first and second radial and short extensor carpal.

NCT ID: NCT03896204 Completed - Epicondylitis Clinical Trials

Effect of Telephone-supported Joint Protection Technique Training

Start date: March 29, 2019
Phase: N/A
Study type: Interventional

There is limited evidence of the efficacy of joint protection principles in individuals diagnosed with lateral epicondylitis in the literature. The aim of this study was to investigate the effect of training of the telephone supported joint protection technique education on pain and upper extremity function in individuals with lateral epicondylitis. New information will be obtained according to the results.

NCT ID: NCT03380559 Completed - Epicondylitis Clinical Trials

A Phase III Study to Evaluate Efficacy of Botulinum Toxin for Treating Epicondylitis

EPITOX
Start date: April 19, 2019
Phase: Phase 3
Study type: Interventional

The study aims to demonstrate that intramuscular injection of botulinum toxin with a paralyzing dose coupled with subcutaneous injection of corticoid has greater efficacy than corticoid injection only or toxin injection only for treating lateral epicondylitis in reducing pain at 6 months. As secondary objectives, the study aims to - demonstrate improvement of quality of patient's life and positive effect on their resuming to professional activities or sportive activities. - evaluate tolerance of treatment by grip strength measurement and adverse event collection.

NCT ID: NCT03225404 Completed - Epicondylitis Clinical Trials

Effectiveness of Percutaneous Electrolysis in the Treatment of Lateral Epicondylalgia. A Single-Blind Randomized Controlled Trial.

MRH
Start date: July 18, 2018
Phase: N/A
Study type: Interventional

The concept of epicondylitis refers to the manifestation of pain ni the area of insertation of the epicondile muscles, and that it is accompained by limitation funcional.A tendinopathy is characterized as a process of degenaration, with fibroblast proliferation and disorganization of the fibers of collagen. This tendon pathology especially affects the epicondyle extensors and especially the first and second radial and short extensor carpal.

NCT ID: NCT02378285 Completed - Epicondylitis Clinical Trials

Treatment of Epicondylitis by Ultrasound-guided Local Injections of PRP (Platelet Rich Plasma)

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

The purpose of this study is to assess efficacy of two intra-tendinous injections of platelet-rich plasma (PRP) on epicondylitis of recent evolution (≤ 3 months) compared compared to two intra-tendinous injections of saline solution (placebo).

NCT ID: NCT01945528 Completed - Epicondylitis Clinical Trials

Platelet Rich Plasma (PRP) in Chronic Epicondylitis

B-PRPtendon
Start date: April 2014
Phase: Phase 3
Study type: Interventional

Background Tendinopathy is a difficult problem to manage and can result in significant patient morbidity. Currently, the clinical use of PRP in painful tendons is widespread but its efficacy remains controversial. Current experimental research postulates different efficiency among PRP formulations.Recent reviews showed that most clinical studies in tendinopathies have been performed with L-PRP. The investigators aim to examine the efficacy of pure-PRP in the management of epicondylitis. The investigators hypothesized that pure PRP associated to needling intervention can enhance tendon healing in epicondylitis, improve function and reduce pain. Methods and design Randomized double blind controlled trial, a total of 80 patients will be randomly allocated into one of two groups: PRP or control. Interventions: PRP group, ultrasound (US)guided needling associated to delivery of multiple PRP depots each alternate week for a total of two interventions. Control Group: US-guided needling with lidocaine each alternate week for a total of two interventions. Main outcome measure: Changes in pain and activity levels, as assessed by Disabilities of the Arm, Shoulder and Hand (DASH)outcome measure score, before and six months after intervention.The primary end-point is 25% reduction in DASH. The investigators will compare the percentage of patients, in each group, that achieve a successful treatment defined as a reduction of at least 25% in the DASH score. Secondary outcome measures:Changes in pain and function as assessed by DASH and changes in pain as assessed by the visual analogue scale (VAS)at the 3, 6 and 12 month follow-up. Changes in sonographic features and neovascularity at 3, 6 and 12 months.

NCT ID: NCT00382941 Completed - Tendinopathy Clinical Trials

Study of LED Phototherapy for Musculoligamentous Lesions

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether LED phototherapy using combined red and near infrared light (approved: Ministry of Health of Russian Federation No. 29/06070997/1080-00, EUROCAT Certificate No. CP033321-IV) is effective in the treatment of musculoligamentous lesions in physiotherapy practice