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Clinical Trial Summary

The purpose of this study is to investigate whether daily use of a microcurrent neuromodulation device, which applies a small current of electricity to the forehead and maxillary region, will decrease the pain experienced by patients in the days following functional endoscopic sinus surgery (FESS). This study is a prospective randomized controlled study. Enrolled subjects will be randomized (1:1) to receive either an active neuromodulation study device or a sham device that appears identical to the active device while emitting no therapeutic microcurrent. Subjects will self-treat with the device at home and will be followed for 2 weeks after FESS.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05198518
Study type Interventional
Source Icahn School of Medicine at Mount Sinai
Contact Chanel Rojas
Phone (347) 962-6630
Status Recruiting
Phase N/A
Start date February 1, 2022
Completion date February 2024

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