Follow-up of the Rotator Cuff Calcific Tendonitis trial: - Needle US-guided treatment vs. Subacromial corticosteroids

Completed

• Conditions: calcifying tendonitis; shoulder calcific depositis; 10043237

• Registration Number: NL-OMON42504
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 48

Inclusion Criteria

Included in original RCCT trial (P09.239)

Exclusion Criteria

none

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Mid-term Constant Score (4-5 years).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>WORC, DASH, VAS scores for pain, anchor questions, aspect, location and<br /><br>classification (including Gärtner score) of eventual calcifications and the<br /><br>state of the rotator cuff (e.g. tendonitis or rupture y/n).</p><br>