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Frozen Shoulder clinical trials

View clinical trials related to Frozen Shoulder.

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NCT ID: NCT04831255 Recruiting - Adhesive Capsulitis Clinical Trials

ZILRETTAâ„¢ for Treatment of Idiopathic Adhesive Capsulitis

Start date: June 21, 2019
Phase: Phase 1
Study type: Interventional

Adhesive capsulitis is a fairly common orthopedic condition that causes pain and loss of range of motion. There are a variety of ways to treat adhesive capsulitis, one of them being an intra-articular steroid injection. This is done to help decrease the inflammatory response caused by adhesive capsulitis. In this study, all participants will receive an intra-articular glenohumeral injection of ZILRETTA and will be followed up with at four time points over 1 year to observe pain, function and range of motion following the injection.

NCT ID: NCT04806191 Recruiting - Shoulder Pain Clinical Trials

Simple and Evidence-based Examination and Treatment of Shoulder Pain in General Practice

EASIER
Start date: March 11, 2021
Phase: N/A
Study type: Interventional

Previous research suggests that general practitioners find handling patients with shoulder pain difficult and that the current care for shoulder pain is not in line with the best available evidence (1).This project aims to assess the effectiveness, costs and implementation of an evidence-based guideline for shoulder pain in general practice.

NCT ID: NCT04802213 Recruiting - Frozen Shoulder Clinical Trials

Invention of Portable Laser Acupuncture and Joint Mobilization Device on Frozen Shoulder and Therapeutic Effects

Start date: March 20, 2021
Phase: N/A
Study type: Interventional

the volunteers with frozen shoulder will be recruited to this experiment and use devices under a designed experimental procedure. After subjects use device , R&D team will collect subject feedback, efficacy assessments, and various device data. This step will not only help investigators to improve and refine the device but also find the best operating mode and using standard of the device to help the frozen shoulder patients. Subjects in this study will also enter a designed course of treatment. All patients will be distributed equally and randomly to three groups (control , mobilization device, laser acupuncture plus mobilization device) to receive treatment. All groups receive three therapy sessions per week for 8 consecutive weeks. At last, investigators will compare the differences between the three groups to understand the effect of portable laser acupuncture and joint mobilization device on frozen shoulder.

NCT ID: NCT04758585 Completed - Depression Clinical Trials

Non-adherence to Pain Medication Increases Risk of Postoperative Frozen Shoulder

NaFS
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Background: Postoperative Frozen-Shoulder (FS) or adhesive capsulitis is a relatively frequent complication (5-20%), even after simple arthroscopic shoulder surgeries. The pathophysiology is still unclear, but psychological factors may play a pivotal role. From clinical experience, the investigators hypothesized that participants, who are reluctant to take medications, particularly "pain-killers", have an increased incidence of postoperative FS. The investigators retrospectively compared participants with and without postoperative FS by their attitude towards medication and by depression scale questionnaires.

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: 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: 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).

NCT ID: NCT04619173 Completed - Frozen Shoulder Clinical Trials

Additional Effects of Thoracic Manipulation in Adhesive Capsulitis.

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to measure the additional effects of thoracic manipulation on pain and restricted shoulder mobility and reducing disability in patients with adhesive capsulitis. A randomized control trail is conducting at Helping hand institute of rehabilitation sciences Mansehra. Patients diagnosed with frozen shoulder were randomized into 2 groups i.e. Group A (n=16) and Group B(n=16) with the help of lottery method. Group A would receive conventional therapy including hot pack, transcutaneous electrical nerve stimulation, stretches and facilitation techniques Group B would receive thoracic manipulation along with hot pack and TENS, stretches and facilitation techniques. The total treatment time is 2 weeks with three sessions per week making a total of 6 sessions. Baseline assessment on 1st visit. 2nd assessment on 6th visit. 3rd assessment on follow up after 3 weeks would be done. The study duration is 6 months. Purposive non probability sampling technique applied. Only 40 to 60 years participants with adhesive capsulitis are including in this trial. Tools use in this study are visual analogue scale (VAS), bubble inclinometer and (disability of arm, shoulder and hand) questionnaire. Data analyzed through statistical package of social sciences version 25.