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Clinical Trial Summary

Assess the clinical outcomes using atelocollagen injection in patients with calcific tendinitis.


Clinical Trial Description

Suitable participants based on the selection/exclusion criteria are randomly assigned to either the case group or the control group. Consent is given right before the procedure. Case group (Atelocollagen injection group): Ultrasound-guided barbotage followed by lidocaine and atelocollagen injection. Control group (Lidocaine injection group): Ultrasound-guided barbotage followed by lidocaine injection." Clinical outcomes will be assessed with functional scores on 6 months after injection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06040112
Study type Interventional
Source The Catholic University of Korea
Contact
Status Recruiting
Phase Phase 4
Start date December 6, 2023
Completion date June 2025