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Standardizing clinical trials for synthetic matrices in rotator cuff tears

Clinical reports on synthetic matrices for rotator cuff tears (RCTs) have varied outcomes owing to limitations such as inconsistency in follow-up time, small sample sizes and lack of control groups. Standardized methods are crucial to optimize synthetic matrix applications and ensure consistent results in tendon repair.

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Acknowledgements

This work was supported by funding from 1332329/EFRI/NSF. The authors thank D. Ghosh for manuscript editing and helpful discussions.

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Correspondence to Cato T. Laurencin.

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C.T.L. is on the board of directors of Alkermes and Mimedx companies. He is an owner of Healing Orthopaedic Technologies-Bone Inc.

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Mirdamadi, E.S., Attari, S. & Laurencin, C.T. Standardizing clinical trials for synthetic matrices in rotator cuff tears. Nat Rev Bioeng 3, 441–443 (2025). https://doi.org/10.1038/s44222-025-00292-8

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