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Adhesive Capsulitis clinical trials

View clinical trials related to Adhesive Capsulitis.

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NCT ID: NCT04561310 Completed - Adhesive Capsulitis Clinical Trials

Comparison of PFS and ART in Adhesive Capsulitis in Diabetic Patients

Start date: June 15, 2020
Phase: N/A
Study type: Interventional

To determine the technique that will have better effects in realigning the muscle kinematics and to normalize the muscle activity along with reducing muscle stiffness with mobilizations techniques

NCT ID: NCT04549051 Completed - Adhesive Capsulitis Clinical Trials

Percutaneous Interruption of the Coracohumeral Ligament for the Treatment of Frozen Shoulder

CHLTenex
Start date: November 17, 2020
Phase: N/A
Study type: Interventional

Percutaneous Interruption of the Coracohumeral Ligament for the treatment of Frozen Shoulder.

NCT ID: NCT04496167 Completed - Adhesive Capsulitis Clinical Trials

Safety and Efficacy of EN3835 in Participants With Frozen Shoulder

Start date: July 29, 2020
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety and efficacy of EN3835 for the treatment of adhesive capsulitis of the shoulder (frozen shoulder).

NCT ID: NCT04413162 Recruiting - Shoulder Pain Clinical Trials

Using Kinect Motion Capture to Measure Shoulder Motion in Patients Undergoing Capsular Distension for Adhesive Capsulitis

Start date: June 10, 2020
Phase: N/A
Study type: Interventional

This study will compare shoulder range of motion assessment using the Kinect motion tracking system vs goniometer in patients with adhesive capsulitis (frozen shoulder) undergoing ultrasound-guided capsular distention procedures (standard of care). The investigators hypothesize that, for shoulder adhesive capsulitis, the Kinect Motion Analysis 2.0 system will provide reliable results in a shorter and more efficient amount of time in comparison to traditional goniometer methods.

NCT ID: NCT04364425 Recruiting - Adhesive Capsulitis Clinical Trials

Steroid Injection for Adhesive Capsulitis

Start date: May 4, 2020
Phase: N/A
Study type: Interventional

This study was conducted to compare the efficacy of hydrodilatation with low dose steroid with high dose steroid for treating adhesive capsulitis.

NCT ID: NCT04160091 Terminated - Adhesive Capsulitis Clinical Trials

Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis

Start date: November 7, 2019
Phase: Phase 2
Study type: Interventional

This is a double-blind study to evaluate the efficacy and safety of FX006 in patients with glenohumeral osteoarthritis (OA) or shoulder adhesive capsulitis (AC).

NCT ID: NCT04157387 Completed - Adhesive Capsulitis Clinical Trials

Cyriax Inferior Capsule Stretching in Idiopathic Adhesive Capsulitis

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

The objective of study is to find out the effectiveness of cyriax capsular stretching in idiopathic adhesive capsulitis and to find out the combined effect of capsular stretching's, mobilization and conservative treatment on pain and Range of Motion (ROM) in idiopathic adhesive capsulitis.

NCT ID: NCT03951896 Completed - Adhesive Capsulitis Clinical Trials

Efficacy of Platelet Rich Plasma Injections in Patients With Adhesive Capsulitis of the Shoulder

Start date: May 3, 2014
Phase: Early Phase 1
Study type: Interventional

This study was done to investigate whether platelet rich plasma(PRP) injections are effective in the management of adhesive capsulitis of the shoulder(AC).Patients were randomized to 2 groups, and one group took PRP injections for 3 times every two weeks, while the other group took saline injections in same frequency and volume. A standardized exercise programme was also applied to all patients. Patients were then evaluated with Shoulder Pain and Disability Index(SPADI), Visual analogous scales for pain and disability, Ranges of Movements and use of analgesics in before, after and 3rd month of the therapy.

NCT ID: NCT03791892 Completed - Adhesive Capsulitis Clinical Trials

Shoulder Mobilization Following Supra Scapular Nerve Block in Adhesive Capsulitis

Start date: December 15, 2018
Phase: N/A
Study type: Interventional

Those shoulder patients who fulfill inclusion criteria are divided into two groups. Supervised exercises will be performed by both groups. Kaltenborn mobilization will be applied to patient in experimental group only. Assessment will be done on baseline, 7th and post visit. A total 38 subjects were included in study who met inclusion criteria. Number of patients in both groups was 19.

NCT ID: NCT03770546 Withdrawn - Adhesive Capsulitis Clinical Trials

Amnion-Based Injections in the Shoulder

Start date: October 30, 2021
Phase: N/A
Study type: Interventional

Osteoarthritis (OA) of the shoulder is a common debilitating condition affecting up to 5% of the general population and as much as 32% of patients over 60 years of age. Clinically, OA is diagnosed by a combination of symptoms, such as slow onset of progressively worsening shoulder pain and stiffness over months to years (often with a history of minor trauma), and pain with activity. Physical exam may show tenderness and swelling, muscle atrophy, and decreased range of motion. Adhesive capsulitis (also called "Frozen Shoulder") is another common shoulder condition, affecting 2-5% of the general population. Frozen shoulder presents with a similar combination of symptoms, such as inability to sleep on the side of the affected shoulder, shoulder pain, and pain at extremes of active and passive range of motion. Despite the ubiquitous nature of these conditions, various non-operative treatment modalities have been employed in their managements without a clearly superior alternative. The usual initial treatment strategy for both of these conditions is the same: a trial of conservative management. Conservative management includes physical therapy, supervised neglect, over-the-counter pain medications (including NSAIDs, like Advil), oral and intra-articular corticosteroid use (steroids), hydrodilatation (capsular distension to rupture), intra-articular hyaluronic acid injections. Despite several years of employing different modes of treatment, there is no evidence that places one treatment modality over the others, and patients will often need surgery. Amniotic fluid's apparent ability to improve blood flow, re-organize collagen, and protect cartilage makes it theoretically ideal for disorders like osteoarthritis and frozen shoulder. In recent studies, it has shown efficacy in promoting ligament healing in the knee and promoting tendon and degenerative joint pain reduction and functional improvement. It has been useful as a material for cartilage repair when used as a scaffold. Intra-articular amnion membrane injection may have favorable outcomes in patients with osteoarthritis of the shoulder or frozen shoulder. To test this hypothesis, intra-articular amnion will be injected into the shoulders of 20 patients with moderate to severe osteoarthritis and 20 patients with frozen shoulder. The hypothesis is that improvement in short-term outcomes (pain, function, and range of motion) will be identified following amnion injection in these patients. The goal of this study is to lead to larger randomized controlled trials evaluating amnion against current forms of treatment for osteoarthritis.