Clinical Trials Logo

Clinical Trial Summary

The primary goal of the study is to assess ultrasonographic Power Doppler signals after ultrasound-guided puncture and lavage of rotator cuff calcific tendinitis of the shoulder. Secondary outcomes are sonographic features like the course of residual calcific material and the course of tendon healing als well as the clinical symptoms of the patient.


Clinical Trial Description

In our study we investigate the intensity of the power doppler signal after ultrasound-guided puncture and lavage (UGPL) of the rotator cuff calcific tendinitis. We assume that UGPL will lead to intratendinous neovascularisation and that the amount of retrieved calcific material is associated with the PDUS signal. The measurement of the signal will be performed in pre determined time slot for 12 months. Additional we study the correlation between the PDUS signal and the clinical symptoms of the patient and the healing process. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05264935
Study type Observational
Source Schulthess Klinik
Contact Laurent Audigé, Prof
Phone +41443857580
Email forschung.oe@kws.ch
Status Recruiting
Phase
Start date May 1, 2022
Completion date April 1, 2024

See also
  Status Clinical Trial Phase
Withdrawn NCT03319784 - Analysis for NSAID VS Corticosteroid Shoulder Injection in Diabetic Patients Phase 4
Not yet recruiting NCT06023914 - Analysis of the Effect of Neuromuscular Electro-stimulation on the Performance of Isometric Rotator Cuff Strength. Phase 2/Phase 3
Completed NCT01984203 - Rotator Cuff Tendinopathy Exercise Trial N/A
Completed NCT01402011 - Study of 25% Dextrose Injections in Shoulder Ligaments and Tendons to Promote Their Healing N/A
Completed NCT01355549 - Platelet-Rich Plasma Therapy for Shoulder Pain in Persons With Spinal Cord Injury Phase 1
Terminated NCT00764764 - Study of the Effect of Neck Treatment on Shoulder Impingement Phase 1
Completed NCT03892603 - Does The Type of Exercise Influence Outcome in Rotator Cuff Related Shoulder Pain N/A
Active, not recruiting NCT03752827 - Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears N/A
Recruiting NCT02967640 - Does Subacromial Injection With Glutamate Receptor Antagonist, Ketamine, Attenuate Pain in Rotator Cuff Tendinopathy? Phase 2/Phase 3
Terminated NCT04115644 - Effectiveness of Corticosteroid vs. Ketorolac Shoulder Injections: A Prospective Double-Blinded Randomized Trial Phase 4
Completed NCT03425357 - Sonoelastography of the Supraspinatus Tendon N/A
Completed NCT03425344 - Discriminative Validity of Strain Elastography of the Supraspinatus Tendon N/A
Recruiting NCT04923477 - Therapeutic Exercise for Rotator Cuff Tendinopathy / Subacromial Pain Syndrome - Outcomes and Mechanisms N/A
Not yet recruiting NCT06372600 - Effect of Extracorporeal Shock Wave Combined With Autologous Platelet-rich Plasma Injection on Rotator Cuff Calcific Tendinitis N/A
Completed NCT03675399 - Effect of Isometric Exercise on Pain Perception in Rotator Cuff Related Shoulder Pain N/A
Recruiting NCT05489484 - Performance and Safety Evaluation of MD-Shoulder Collagen Medical Device in the Treatment of Rotator Cuff Syndrome N/A
Recruiting NCT04094298 - Use of Extended Release Triamcinolone in the Treatment of Rotator Cuff Disease Phase 3
Active, not recruiting NCT03167138 - Micro-Fragmented Adipose Tissue (Lipogems®) Injection for Chronic Shoulder Pain in Persons With Spinal Cord Injury Early Phase 1
Completed NCT03567109 - Body Schema Alterations in Musculoskeletal Disorders : Effect of Laterality
Recruiting NCT05235152 - Group-based Exercise Training Programs for Military Members With Musculoskeletal Conditions N/A