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Bursitis clinical trials

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NCT ID: NCT05311839 Completed - Clinical trials for Adhesive Capsulitis of Shoulder

Effect of Thera Band Exercises on Adhesive Capsulitis Post Mastectomy

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

Breast cancer surgeries particularly mastectomy results in limited shoulder movement which can lead to arm, shoulder pain and stiffness. Females who underwent mastectomy have reported a significantly higher incidence of shoulder morbidity

NCT ID: NCT05299242 Completed - Frozen Shoulder Clinical Trials

The Anti-Freaze-F Study- "Anti-TNF for Treatment of Frozen Shoulder - a Feasibility Study"

Anti-FreazeF
Start date: July 21, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

Frozen shoulder is a common condition affecting approximately 9% of people aged 25-64 years. During the early phase the pain is usually unbearable and the later restriction in movement is severely limiting. It occurs when the flexible tissue (capsule) that surrounds the shoulder joint becomes inflamed, thickened and tight. The pain can be very severe and lasts 3-9 months, followed by a 4-12 month period of increasing stiffness, after which the condition usually improves. Frozen shoulder often affects a person's ability to sleep, carry out everyday activities, and work. Current treatments include rest, painkillers, anti-inflammatories, physiotherapy and steroid injections. If stiffness persists, surgery is sometimes recommended. However, there is no evidence that any of these treatments lead to significant benefit in the long term, with many being ineffective. The aim of this study is to find out if it is possible to run a larger trial to test whether an injection of adalimumab can reduce pain and prevent the disease from getting worse, if given during the early painful phase of frozen shoulder. The investigators need to conduct this smaller study first to be sure it's possible to identify and treat people with early stage frozen shoulder, before they conduct a much larger trial to find out if this treatment works. In this study the investigators will include 84 adults from 5 sites with painful early stage frozen shoulder who have not yet received treatment. People will be randomised to receive either an injection of the drug adalimumab or a dummy injection of saline (placebo) directly into the shoulder joint, both guided by ultrasound. All participants will also receive standardized advice on how to manage their shoulder pain. The investigators will assess participants before treatment and three months later. Adalimumab has been used very successfully to treat other inflammatory diseases such as rheumatoid arthritis. This study has been funded by the NIHR RfPB programme and 180 Life Sciences.

NCT ID: NCT05292482 Completed - Adhesive Capsulitis Clinical Trials

Pragmatic Randomized Controlled Trial of Pharmacopuncture Therapy for Adhesive Capsulitis : A Pilot Study

Start date: April 20, 2022
Phase: N/A
Study type: Interventional

This is a 2-arm parallel pragmatic randomized controlled trial that will compare pharmacopuncture therapy with physical therapy for adhesive capsulitis.

NCT ID: NCT05290272 Recruiting - Knee Osteoarthritis Clinical Trials

Validity of AI in Treatment of the Musculoskeletal Conditions by Vifive

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of the 12-week ViFive program, a vision-based artificial intelligent digital care plan for chronic knee pain. ViFive digital care plan is delivered by a physical therapy team consisting of physical therapists and a personal coach. We aim to understand the safety and efficacy of this vision artificial intelligent based home exercise program.

NCT ID: NCT05274698 Recruiting - Clinical trials for Adhesive Capsulitis of Shoulder

Efficacy Of Muscle Energy Technique On Shoulder Adhesive Capsulitis Post Mastectomy

Start date: February 1, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the effect of muscle energy technique on adhesive capsulitis post mastectomy.

NCT ID: NCT05230667 Recruiting - Adhesive Capsulitis Clinical Trials

Comparison of the Effect of Combined Glenohumeral Joint and Subdeltoid Bursa Injection With Platelet-rich Plasma (PRP), Corticosteroid, and Normal Saline in Addition to Physical Therapy for Treatment of Frozen Shoulder

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

Frozen shoulder, adhesive capsulitis, shoulder, platelet-rich plasma, corticosteroid, injection.

NCT ID: NCT05214547 Recruiting - Adhesive Capsulitis Clinical Trials

Effectiveness of Focal Vibration in Shoulder Pathology

FVinAC
Start date: February 25, 2022
Phase: N/A
Study type: Interventional

We hypothesize that focal vibration therapy will reduce pain, increase the mobilization of the glenohumeral joint, and will improve functionality in patients with adhesive capsulitis.

NCT ID: NCT05213351 Completed - Adhesive Capsulitis Clinical Trials

Two Different Exercise Training in Frozen Shoulder Treatment

Start date: April 25, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of two different exercise programs in patients with frozen shoulders.

NCT ID: NCT05212740 Completed - Frozen Shoulder Clinical Trials

Oral Corticosteroids Versus Exercises On Treatment Of Frozen Shoulder,

Start date: January 25, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of exercise and oral corticosteroids the treatment of a FS.

NCT ID: NCT05210036 Completed - Clinical trials for Adhesive Capsulitis of Shoulder

HILT and US Therapies in Adhesive Capsulitis

Start date: November 15, 2015
Phase: N/A
Study type: Interventional

Background: Adhesive capsulitis (AC) is a common musculoskeletal disease characterized by pain and limitation of movement in the shoulders of patients. Purpose: This study aimed to assess the effectiveness of short- and long-term therapeutic ultrasound (US) and high-intensity laser therapy (HILT) in the treatment of AC. Methods: A total of 60 patients with AC were randomized into two groups. Group I received US (15 sessions in total) and Group II received HILT (9 sessions in total) for 3 weeks. In addition, all the patients received 15 sessions of physical therapy programs (hot pack, TENS and therapeutic exercises). Assessments were made using VAS-Pain, Shoulder Pain and Disability Index (SPADI) and range of motion (ROM) with goniometer before and at the end of the treatment and in the posttreatment 1st and 6th months.