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Clinical Trial Summary

This feasibility and non-randomized comparison study explores the possible benefits of splint design and production by 3D-printing in a clinical setting and looks at splint users' experiences with customizable 3D-printed finger splints compared to conventionally made splints. Fifty participants with a hyperextended finger condition are assigned by researcher to either an interventional group (customizable 3D-printed finger splint) or a control group (conventional thermoplastic finger splint). Participants will wear assigned splint for 1 month. Functional status and satisfaction with splint will be assessed at the end of the 1-month duration in the form of surveys on satisfaction and functional status participants will be asked to complete. The findings will contribute to evidence that customizable 3D-printed finger splints can serve as a feasible, cost-effective option to improve patient satisfaction and functional status. It will further justify the need for the application of 3D-printing in a clinical setting.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05903391
Study type Interventional
Source NorthShore University HealthSystem
Contact Natasha Irani, OTD, BA
Phone 773-878-8200
Email nirani@schosp.org
Status Recruiting
Phase N/A
Start date November 9, 2023
Completion date December 31, 2025