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Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece

Hair Removal Clinical Trial

Official title:
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece

Clinical Trial Summary

The objective of this clinical study is to verify hair count reduction, associated comfort/discomfort and treatment time using the LightSheer Duet System with the High Speed (HS) handpieces for temporary hair removal and permanent hair reduction. It is anticipated that the larger treatment size of the HS handpiece will result in faster treatment of larger areas; and that the lower energy levels will result in greater comfort.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01282866
Study type Interventional
Source Lumenis Ltd.
Contact
Status Completed
Phase N/A
Start date June 2009
Completion date November 2011
View Details
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