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Clinical Trial Summary

This study aims to evaluate the safety and the efficacy of applying transcutaneous trigeminal nerve stimulator (NuEyne P01) on autism spectrum disorder.


Clinical Trial Description

Duration of study period (per participant): Screening period (-28~0 days), Intervention period (28 days) Patient needs to visit site at least 4 times (V1, V2, V4, V6). V2 can be done with V1. Tele-visit should be done on V3 (day 7), V5 (day 21). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06233279
Study type Interventional
Source Nu Eyne Co., Ltd.
Contact Jinho Jung, Ph.D candi.
Phone +821083113509
Email jinho.jung@nueyne.com
Status Recruiting
Phase N/A
Start date November 15, 2022
Completion date August 30, 2024

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