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Thaler, Roman

0000-0001-5515-8719

Mayo Clinic

Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.

Citations 1

Design and validation of a biomechanics device for preclinical arthrofibrosis models
Carstens, Mason , Meißner, Nils , Weintraub, Matthew T. , Pichurin, Oksana , Morrey, Mark E. , Sánchez‐Sotelo, Joaquín , Thaler, Roman , Abdel, Matthew P. , Carstens, Mason F. , Thaler, Roman , Abdel, Matthew P , Meissner, Nils , Sanchez-Sotelo, J. , Morrey, Mark E , Berry, Daniel J.

Bone & Joint Research | June 19, 2026 | Volume: 15 | Issue: 6 | Pages: 716-725

10.1302/2046-3758.156.bjr-2025-0620.r1 Get It

Aims Reliable assessment of joint stiffness is essential for studying arthrofibrosis in preclinical animal models. This study presents a new dedicated biomechanics device for measuring knee stiffness in mouse, rat, and rabbit models of arthrofibrosis, with the aim of validating its performance and comparing it to a previously validated device. Methods The new system integrates a torque load cell, stepper motor, and absolute encoder in a through-hole, unified configuration for precise continuous torque-angle measurement, with custom limb brackets ensuring species-specific alignment at the joint’s centre of rotation. To validate this device and compare it to a previously validated device, arthrofibrosis was induced using established models of extra-articular immobilization in mice and intra-articular violation with immobilization in rats and rabbits, followed by defined remobilization periods. Torque-angle curves were recorded ex vivo across species-specific torque ranges, and measurement variability between the new and a previous validated device was statistically compared using Brown-Forsythe’s test. Results The onset of hyperextension in contralateral limbs occurred at mean angles of 152.4° (mice), 154.4° (rats), and 152.8° (rabbits), and at maximum torque, mean flexion angles were 79.2°, 87.3°, and 140.5°, respectively. No significant differences in measurement variability were observed between devices across all species. Conclusion These findings demonstrate that our new device provides reproducible torque-angle data while maintaining the statistical robustness of the previous device and offering improved mechanical design and operational standardization. By enabling standardized, cross-species joint stiffness quantification, this platform improves cross-study comparability and strengthens the translational reliability of preclinical arthrofibrosis research. Cite this article: Bone Joint Res 2026;15(6):716–725.