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Clinical Trial Summary

To measure the safety of hair removal device when used frequently.


Clinical Trial Description

The primary endpoint of this study is to measure the safety of the Hair2Go device when used frequently. The secondary endpoints include the kinetics of the hair clearance up to 8 weeks after the last treatment, and gathering information about the pain associated with the procedure ;


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01348789
Study type Interventional
Source Syneron Medical
Contact
Status Completed
Phase N/A
Start date March 2011
Completion date June 2012

See also
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Completed NCT01348776 - The Efficiency of the Hair2Go Device: A Prospective, Open, Label Study With Before-After Design N/A
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