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Clinical Trial Summary

In this study we will see if application of TENS for a period of 30 minutes in addition to ibuprofen reduces the pain of emergency department patients with back pain compared with ibuprofen and a sham TENS unit.


Clinical Trial Description

Adult patients presenting to the emergency department with moderate to severe back pain of relatively short duration without neurological deficits will be eligible for inclusion in the study. After signing informed consent the patients will rate their pain severity and receive a 400 mg dose of ibuprofen and then randomly be assigned to either TENS or sham TENS for 30 minutes. At the end of the study period patients will again be asked to rate their pain severity and indicate whether their pain got better or worse. We will also ask them to try and guess which treatment they received and whether they require any medications for their pain. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04227067
Study type Interventional
Source Stony Brook University
Contact
Status Completed
Phase N/A
Start date January 20, 2020
Completion date February 12, 2024

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