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Clinical Trial Summary

The purpose of this study is to assess the efficacy of using a percussive therapy device in addition to physical therapy to treat acute tennis elbow


Clinical Trial Description

The device the investigators intend to use is Class I and in a class of devices that is exempt from the FDA requirement for premarket notification/approval (exempt from 510K or PMA), which would not be "subject to section 510(k), 515, or 520(m) of the Federal Food, Drug, and Cosmetic Act" (ref: FDAAA Checklist) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05723809
Study type Interventional
Source Cedars-Sinai Medical Center
Contact Joshua Langberg, B.A
Phone 8184423333
Email joshua.langberg@cshs.org
Status Not yet recruiting
Phase N/A
Start date March 1, 2023
Completion date September 1, 2023

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