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Clinical Trial Summary

Evaluation of clinical and radiological outcomes in patients undergoing Arthroscopic Rotator Cuff Repair with standard treatment compared to patients receiving biological stimulation with micro-perforations or with the combination of micro-perforations and use of Artelon® Tissue Reinforcement, a synthetic device based on degradable polyurethaneurea.

The investigators believe that this kind of tendon-to-bone healing stimulation with the two proposed methods can increase the repair quality by significantly decreasing the lesion recurrence rate (currently described for 15% of patients) and can improve various parameters such as pain, range of motion and strength, thereby hastening the return to daily activities and psycho-physical well-being.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03060928
Study type Interventional
Source ASST Gaetano Pini-CTO
Contact
Status Not yet recruiting
Phase N/A
Start date March 1, 2017
Completion date December 31, 2020

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