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Tendinopathy clinical trials

View clinical trials related to Tendinopathy.

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NCT ID: NCT01833598 Completed - Clinical trials for Chronic Tendinopathy

Percutaneous Needle Tenotomy (PNT) Versus Platelet Rich Plasma (PRP) With PNT in the Treatment of Chronic Tendinosis

Start date: September 2012
Phase: N/A
Study type: Interventional

Tendinopathy is a clinical syndrome of chronic pain and tendon degeneration that impairs a person's ability to perform daily activities and recreation. Traditional conservative treatments include activity modification, exercises, ice/heat, and medications and corticosteroid injection. A newer treatment is percutaneous needle tenotomy (PNT), in which the affected area is repetitively needled to disrupt pathological tissue and induce bleeding. This turns a nonhealing chronic injury into an acute injury with enhanced healing capability. Another is Platelet Rich Plasma (PRP), whereby patients' own platelets are injected into the affected area, also activating growth factors. There has been promising research in these tendinopathy treatments but more research is needed. The investigators plan to expand on prior studies to identify a reproducible and efficacious treatment for chronic tendinopathy to reduce pain and improve function and quality of life. Our goal in this study is to assess the efficacy of ultrasound guided (USG) PNT versus PNT with peritendinous PRP as a treatment for chronic tendinopathy.

NCT ID: NCT01832376 Completed - Calcific Tendinitis Clinical Trials

Treatment of Calcific Tendinitis by Ultrasound-guided Needle Lavage

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

Study population: Subjects with long standing symptoms from calcific tendonitis, non-responsive to other forms of conservative treatment Study method: A cohort of 50 patients with symptomatic calcific tendonitis will be treated by ultrasound-guided needle lavage. At baseline all study subjects will be assessed by clinical examination, imaging of the shoulder by x-ray and sonography and by the self-report section of the American Shoulder and Elbow Surgeons score (ASES). Follow-up will be performed after 1 and 4 weeks (score only), 3 (clinical, score, ultrasound, x-ray), 6 and 12 months (score only), and after 24 months (clinical, score, ultrasound, x-ray). Patients with insufficient treatment effect will be offered physiotherapy, re-lavage or surgical treatment by acromioplasty. Purpose of the study: The investigators want to find out - if shoulder function, measured by a shoulder score, will increase during follow-up - how much of the calcific material can be aspirated (in ml) - to which extend the calcific deposit disappears on x-rays and sonographic images - how many patients will need surgical treatment

NCT ID: NCT01692249 Completed - Self Efficacy Clinical Trials

Efficacy and Safety of Spa Treatment in Chronic Shoulder Pain Due to Rotator Cuff Tendinopathy

ROTATHERM
Start date: March 2009
Phase: N/A
Study type: Interventional

To determine whether spa therapy has a beneficial effect on pain and disability in the management of shoulder pain due to chronic rotator cuff lesions, this multicentre randomized prospective clinical trial includes patients with shoulder pain due to chronic degenerative rotator cuff tendinopathy who attend French spa resorts as outpatients. Subjects are randomized into two groups: immediate spa therapy (18 days of standardized treatment) and control (spa therapy delayed for 6 months). All patients continue usual treatments during the 6-month follow-up period. The main endpoint is the mean change in the DASH score at 6 months. Secondary endpoints are the mean change in SF-36 components, treatments used, and tolerance. The effect size of spa therapy is calculated and the proportion of patients reaching minimal clinically important improvement (MCII) is compared between groups.

NCT ID: NCT01691716 Completed - Clinical trials for Achilles Tendinopathy

The Efficacy of Tendoactive, Eccentric Training, and the Combination of Both as a Treatment of Achilles Tendinopathy

Tendoactive
Start date: April 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Tendoactive, eccentric training, or the combination or both could be effective in the treatment of Achilles tendinopathy.

NCT ID: NCT01652495 Completed - Tendinopathy Clinical Trials

Evaluation of Efficacy and Hypothalamus-pituitary-adrenal Axis Suppression Due to Corticosteroids Intrabursal Injection

TPESP2011-12
Start date: March 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy and effects on the hypothalamus-pituitary-adrenal axis of a single intrabursal injection of two different types of corticosteroids (methylprednisolone and triamcinolone) in patients with calcific shoulder tendinopathy.

NCT ID: NCT01612663 Completed - Clinical trials for Complete Tear, Knee, Anterior Cruciate Ligament

Effect of Distal Needling on Knee Pain Using Acupuncture Techniques

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to test if specific therapeutic benefits of acupuncture are mostly attributable to contextual and psychosocial factors, such as patients' beliefs and expectations.The investigators propose using the 2 acupuncture methods, which refrains from inserting needles in the affected area, in order to evaluate the short-term and long-term efficacy of acupuncture in a clinical setting compared with placebo and compared with invasive needling that does not adhere to "correct" acupuncture rules.

NCT ID: NCT01600326 Completed - Tendinosis Clinical Trials

A Prospective Comparison of Ultrasound-Guided Percutaneous Platelet-Rich Plasma Injection

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

The purpose of this study is to determine the effectiveness of various treatment soft tendinosis also known as tendinitis.

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: NCT01460004 Completed - Clinical trials for Patellar Tendinopathy

The Effect of Infrapatellar Strap Treatment on Pain Extent and Athletic Measures in Young Athletes

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is: - To examine the effect of infra patellar strap treatment on the extent of pain and jumping performance tasks in young male athletes diagnosed with patellar tendinopathy. - 40 elite male athletes, basketball and volleyball players, ages 14-18, students of the academy for sports Excellency will take part in this study - Hypothesis 1: The treatment of infra patellar strap will reduce the level of pain during jumping performance tasks. - Hypothesis 2: The treatment of infra patellar strap will improve the squat jump height in athletes with patellar tendinopathy during squat jump task. - Hypothesis 3: The treatment of infra patellar strap will improve the drop jump height in athletes with patellar tendinopathy during drop jump task. - Hypothesis 4: The treatment of infra patellar strap will improve the one leg jump height in athletes with patellar tendinopathy during one leg jump task. - Hypothesis 5: The treatment of infra patellar strap will improve the 30 seconds repetitive jumps mean height in athletes with patellar tendinopathy during 30 seconds repetitive jumps task.

NCT ID: NCT01423682 Completed - Clinical trials for Rotator Cuff Tendinopathy

The Influence of Eccentric Training on the Volume and Vascularisation of the Rotator Cuff in Patients With Rotator Cuff Tendinopathy and Healthy Subjects

Start date: April 2012
Phase: N/A
Study type: Interventional

Patients with rotator cuff tendinopathy make up a large part of the population in physiotherapy practice. The rotator cuff, a shoulder muscle group, plays an important role in causing pain. Tendons suffer large compression and friction, which can lead to degeneration of these tendons. Rehabilitation often leads to unsatisfying results. In Achilles and patella tendinopathy, a new training program called eccentric training has shown very good results. Eccentric training contains exercises during which a force has to be resisted while the muscle lengthens instead of shortens. This would have a larger influence on tendon tissue. Some small studies also show promising results of eccentric training in patients with rotator cuff tendinopathy but the mechanisms behind these results remain unclear. To investigate this, 30 patients with rotator cuff tendinopathy and 30 healthy subjects will be evaluated before and immediately after performing the exercise. Three measurements will be done: ultrasonographic measurement of tendon thickness, power Doppler imaging and measurement of microcirculation around the tendon with Oxygen to see. All measurements are non-invasive, pain free and without risks for the human body.