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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

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