Ignite Creation Date:
2025-12-24 @ 4:37 PM
Ignite Modification Date:
2025-12-26 @ 4:13 AM
Study NCT ID:
NCT01282866
Status:
COMPLETED
Last Update Posted:
2016-10-21
First Post:
2011-01-09
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
Sponsor:
Lumenis Be Ltd.
Organization:
Study Overview
Official Title:
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
Status:
COMPLETED
Status Verified Date:
2014-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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.
Detailed Description:
None
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: