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Bursitis clinical trials

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NCT ID: NCT04756167 Completed - Adhesive Capsulitis Clinical Trials

Effect of Myofascial Relaxation on Individuals With Adhesive Capsulitis

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

In the study, the investigators aimed to investigate the effects of myofascial release method on pain, functionality and quality of life in individuals with adhesive capsulitis. 42 individuals willing to participate in the study will be included. Participants will be randomly divided into two groups, the conventional group and the myofascial release group. Evaluations will be made by another physiotherapist with a single eye blindness. Hotpack, TENS, ultrasound and exercise will be applied jointly to both groups in the study. In addition to the myofascial release group, myofascial release will be applied on the subscapularis and serratus anterior muscles. Individuals will be asked to come to the center where the research will be conducted for a total of fifteen sessions for three weeks, five times a week. Myofascial release will be done in the first five sessions of treatment programs. Participants' pain before the first treatment, at the end of the 5th treatment and after the 15th treatment with Visual Analogue Scale (VAS), shoulder joint range of motion (ROM) with Goniometer, upper extremity functionality level Arm, Shoulder and Hand Problems Questionnaire (DASH) specific shoulder pain and functions will be evaluated with the Shoulder Pain and Disability Index (SPADI), sleep quality with Pittsburgh Sleep Quality Index (PSQI), and quality of life with Short Form-36 (SF-36). Statistical analysis to be used in the investigators study will be made with the Statistical Package for the Social Sciences 20.0 package program.

NCT ID: NCT04747938 Completed - Frozen Shoulder Clinical Trials

Frozen Shoulder Treated by Energy Accumulator

FShouEnAcc
Start date: September 1, 2014
Phase: N/A
Study type: Interventional

Frozen shoulder is a painful and disabling disorder of unclear cause, affecting middle-age people after their 5th decades. They suffer from annoying pain and limited shoulder mobility. Energy Accumulator provides a better way of relief through an integrative medicine concept.

NCT ID: NCT04738253 Recruiting - Frozen Shoulder Clinical Trials

Correlation Between Ultrasonography Finding and Shoulder Range of Motion in Stroke Patients

Start date: November 7, 2020
Phase:
Study type: Observational [Patient Registry]

Limitation of range of motion in the shoulder joints is common in stroke patients. The causes are stiffness, CRPS, and frozen shoulder. The purpose of this study was to investigate the relationship between frozen shoulder and shoulder LOM in patients with cerebral infarction using ultrasonography.

NCT ID: NCT04724317 Completed - Shoulder Pain Clinical Trials

Ultrasound Guided Shoulder Intra-Articular Ozone Injection Versus Pulsed Radiofrequency Application for Shoulder Adhesive Capsulitis

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy of the ultrasound guided shoulder intra-articular Ozone injection versus pulsed radiofrequency application in patients with shoulder adhesive capsulitis. - Primary Outcome : - Pain score using visual analogue scale during rest (VASr) and movement (VASm). - Secondary Outcome : - Quality of life using Shoulder Pain and Disability Index (SPADI). It assesses the overall functionality of the shoulder joint. - Levels of serum ICAM -1, and serum high sensitive C-reactive protein (hs-CRP) are compared before and after treatment intervention.

NCT ID: NCT04715035 Recruiting - Frozen Shoulder Clinical Trials

Efficacy of Eccentric Exercises in Individuals With Frozen Shoulder

Start date: August 3, 2022
Phase: N/A
Study type: Interventional

Frozen shoulder is a musculoskeletal condition with a strong negative impact on activities of daily living, producing pain, disability, anxiety, and sleep disorders. It has a worldwide prevalence of 5.3%, increasing from 10 to 38% in patients with diabetes and thyroid conditions. This clinical entity manifests itself mainly in women between 40 and 65 years of age. Its resolution time is long and can reach 42 months with symptoms that persist throughout life. In the clinical evaluation, patients with Frozen Shoulder are manifested mainly by presenting mobility deficits. Previous studies described different structural alterations that may justify this clinical condition and its consequences, such as, for example, fibrosis of the coracohumeral ligament, alterations of the rotator interval, and of the axillary recess. Although passive structures are believed to be primarily involved in this condition, A series of five cases in which patients with frozen shoulder presented a significant increase in mobility after a general anesthetic block. The data obtained from this study and the different complications presented by patients with CH suggest that it is necessary to further understand the role of the rotator cuff in this clinical condition. Eccentric exercises consist of contracting the muscle to control or decelerate a load while the muscle or tendon is lengthening or remaining stretched. This intervention has been proposed for the treatment of tendinopathies in different body regions.

NCT ID: NCT04709874 Recruiting - Pain, Shoulder Clinical Trials

Paravertebral Block vs. Suprascapular Block for Treatment of Frozen Shoulder

Start date: January 2, 2022
Phase: N/A
Study type: Interventional

Background: Adhesive capsulitis, or frozen shoulder, is a major orthopedic condition that causes pain and functional limitation. Although different nonsurgical conservative therapies such as physical therapy, nonsteroidal anti-inflammatory drugs, and corticosteroid injections have been used, yet there is no standard treatment for frozen shoulder. Objectives: The primary objective of this study is to compare the effectiveness of nerve stimulator guided paravertebral block versus suprascapular block for treatment of frozen shoulder. The primary outcome is pain measured through the Visual Analogue Scale (VAS) over a follow up period of 6 months. Methods: This is a prospective randomized clinical trial that will be conducted between February 2021 and January 2022. Patients will be randomly allocated into two groups. Group I will receive paravertebral block guided by a nerve stimulator. Group II patients will receive suprascapular nerve block. Patients will be followed up at week 1, month 1, month 3 and month 6.

NCT ID: NCT04707274 Completed - Gluteal Tendinitis Clinical Trials

Reliability, Validity, and Cross-cultural Adaptation of the Turkish Version of the Victorian Institute of Sports Assessment for Gluteal Tendinopathy (VISA-G) Questionnaire

Start date: February 10, 2021
Phase:
Study type: Observational

The purpose of this study was to investigate adaptation, validity, and reliability of the Turkish version of the Victorian Institute of Sports Assessment for Gluteal Tendinopathy (VISA-G) Questionnaire.

NCT ID: NCT04692649 Completed - Shoulder Pain Clinical Trials

Comparison of Pragmatic Posterior Capsular Stretch and Crossbody Stretch on the Shoulder Mobility

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Various stretches are used to lengthen the posterior shoulder capsule. No study has reported the comparison of the pragmatic posterior capsular stretch and cross body stertch

NCT ID: NCT04687735 Recruiting - Frozen Shoulder Clinical Trials

Frozen Shoulder Single Arm Prospective Study

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of combination of brachial plexus block plus physical therapy on quality of life improvement in patients with frozen shoulder condition via standard questionnaires.

NCT ID: NCT04680156 Terminated - Adhesive Capsulitis Clinical Trials

Long-term Follow-up Durability (Efficacy) Study of EN3835 for the Treatment of AC of the Shoulder (Frozen Shoulder)

Start date: December 17, 2020
Phase:
Study type: Observational

This is a long-term follow-up study to evaluate the safety and durability (efficacy) of response to EN3835 compared to placebo in participants who were treated in EN3835-210 or the pivotal Phase 3 parent studies for the treatment of AC of the shoulder (frozen shoulder).