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Bursitis clinical trials

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NCT ID: NCT04471259 Completed - Haglund's Deformity Clinical Trials

Functional Follow-up After Endoscopic Calcaneoplasty for Haglund's Deformity

Start date: January 22, 2012
Phase:
Study type: Observational

Isokinetic muscle strength test implemented by the Biodex system is a method used for evaluating muscle function that has been applied clinically in the field of sports and rehabilitation medicine. However, information on its application on Haglund's deformity remain insufficient. Therefore, the present study is designed to examine the effectiveness of the muscle strength test using the Biodex system in evaluating the recovery of athletic capacity in patients with Haglund's deformity following endoscopic surgery.

NCT ID: NCT04454632 Completed - Pain Clinical Trials

The Effect of Mirror Therapy in Patients With Frozen Shoulder

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

The aim of this study compares mirror therapy and visual feedback treatment with the control group in frozen shoulder patients.

NCT ID: NCT04420572 Completed - Clinical trials for Trochanteric Bursitis

Comparison of Ozone and Steroid Injection in Patients With Greater Trochanteric Pain Syndrome

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

Between the large trochanter and the muscles adhering to it, trochanteric bursa and several other bursa may be found. Trochanteric bursitis can be alone or together with tendinitis of other bursa and adhering muscles. The first is called trochanteric bursitis, the second is called hip periarthritis, which is difficult to distinguish clinically. It is more common in women of middle age. The main complaint is the large trochanter and pain on the side of the thigh. Pain is aggregated by walking abduction and external rotation by walking, lying down with hip movements. The palpation is sensitive to the top of the large trochanter. There may also be tenderness in the muscles in the lateral of the thigh. On plain radiographs, slight irregularities or peritrocanteric calcifications can be seen in the large trochanter. Bone scintigraphy shows local increased involvement. In differential diagnosis, stress fractures, local infection and bone and soft tissue tumors should be considered. Rest is recommended in treatment. Activities such as running, standing for a long time are prohibited. Ice application can be given in the acute period. Non-steroidal anti-inflammatory (SOAI) drugs, analgesics, TENS can be used for pain relief. In cases where conventional treatments are insufficient, that is, the patient's pain is still continuing and functional recovery is inadequate, some alternative methods are also applied. These treatments include ozone, prolotherapy injection applications, dry needling, acupuncture, hirudotherapy, phytotherapy, mesotherapy, balneotherapy, kinesiobanding, etc. d. In our study, we aim to compare the effectiveness of ozone injection in patients diagnosed with trochanteric bursitis and to compare steroid injection with the application of ozone therapy.

NCT ID: NCT04369144 Completed - Frozen Shoulder Clinical Trials

Adding Vertical Correction to Scapular Recognition on Patients With Frozen Shoulder

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

OBJECTIVE: To study the effect of adding a continual vertical downward correction to dynamic scapular recognition exercise on scapular dyskinesis and shoulder pain and disability in patients with frozen shoulder. Design: A double-blinded randomized controlled study Setting: Out-patient clinic Subjects: Sixty-seven subjects with unilateral frozen shoulder Interventions: Participants were distributed into two groups. The intervention group performed the dynamic scapular recognition exercise and continual vertical downward correction using rigid taping with 50%-75% tension. The control group performed a similar dynamic scapular recognition exercise using a wireless biofeedback system and placebo taping. A scapular dyskinesis test with caliper was utilized to measure scapular dyskinesis, a digital inclinometer was utilized to evaluate the scapular upward rotation and shoulder ROMs, and the Shoulder Pain and Disability Index (SPADI) was utilized to evaluate the shoulder pain and disability.

NCT ID: NCT04347733 Completed - Clinical trials for Adhesive Capsulitis of Shoulder

Hyaluronidase in Intra-articular Steroid Injection Treating the Adhesive Capsulitis for Shoulder

Start date: May 2, 2017
Phase: Phase 3
Study type: Interventional

Adhesive capsulitis (AC) is painful and disabling condition that is associated with a gradual loss of shoulder motion. Intra-articular steroid injection is a common treatment in the initial painful stage of AC, and its use in combination with hyaluronidase may offer increased therapeutic efficacy owing to synergistic effects. We determined the therapeutic efficiency of the co-administration of hyaluronidase in early AC by evaluating symptomatic, anthropometric, and imaging changes.

NCT ID: NCT04316130 Completed - Frozen Shoulder Clinical Trials

Real-time Interactive Digital Healthcare System in Frozen Shoulder; Randomized Controlled Trial

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

This study aims to examine the effect of hospital-home linkage short-term rehabilitation therapy using real-time interactive digital healthcare system (Uincare Homeplus) in frozen shoulder. This is prospective randomized controlled trial and multi-center study. 100 frozen shoulder who diagnosed with limited range of motion in 2 more plane of flexion, abduction, external rotation of affected shoulder. Shoulder range of motion (ROM), Shoulder Pain and Disability Index (SPADI), pain evaluation with Numeral Rating Scale (NRS), quality of life evaluation with Short Form (SF)-36 Health Survey and EQ-5D-5L, activity daily living (ADL) evaluation with Canadian Occupational Performance Measure (COPM) will be evaluated on enrollment, 4-week, 8-week, 12-weeks, 18-weeks, and 24 weeks after enrollment.

NCT ID: NCT04289922 Completed - Hip Pain Chronic Clinical Trials

Validation of the Norwegian VISA-G Questionnaire

Start date: November 8, 2019
Phase:
Study type: Observational

The aim of this study is to translate, cross-cultural adapt and validate the Norwegian VISA-G (VISA-N-G) questionnaire. The study will test the psychometric properties for the VISA-N-G in terms of test-retest reliability, internal consistency, construct validity and responsiveness.

NCT ID: NCT04182672 Completed - Clinical trials for Trochanteric Bursitis

Study to Assess the Safety and Efficacy of FX006 Administered to Patients With Greater Trochanteric Bursitis

Start date: August 12, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of FX006 in bursal injections and to assess the patient's impression to change in their chronic pain, following treatment.

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: NCT04044196 Completed - Rotator Cuff Tears Clinical Trials

Preoperative Psychological Risk Factors for the Retractable Capsulitis of the Shoulder After Shoulder Rotator Cuff Repair Surgery

Start date: May 1, 2018
Phase:
Study type: Observational

The main objective of our study is to determine whether preoperative anxiety, depression and kinesiophobia are risk factors for retractile capsulitis after arthroscopic rotator cuff repair to best support these patients. patients postoperatively.