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Clinical Trial Summary

- The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction.

- Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site.

- Each subject will receive five treatments at four to six week intervals and return for follow-up visits at three and six months after the last treatment for evaluation of the treated areas.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01801202
Study type Interventional
Source Lumenis Ltd.
Contact
Status Completed
Phase N/A
Start date February 2013
Completion date November 2014

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