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Clinical Trial Summary

To investigate and compare the safety and effectiveness of the ARTAS™ System to manual hair follicle implantation method following a nine month period of post-procedure evaluation.


Clinical Trial Description

This comparative study is a multi-center, prospective, blinded, randomized controlled clinical study where subjects act as their own control.

The purpose of this study is to demonstrate that the ARTAS System is safe and effective for implanting follicular hair units.

Patients will be followed for a nine months period of time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02914587
Study type Interventional
Source Restoration Robotics, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date August 2016
Completion date October 2017

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