At a glance
ClinicalIndex Comparison RecordN/ACompleted· 35 enrolled
Drug / intervention
LightSheer Duetdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
In Brief
A clinical study evaluating LightSheer Duet for Hair Removal. Completed, enrolled 35 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHair Removal
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJun 2009
First PostedJan 2011
Primary CompletionNov 2011
TodayJul 2026
First PostedJan 25, 2011
Enrollment StartJun 1, 2009
Primary CompletionNov 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 15.4 years ago
Interventions
LightSheer Duetdevice
LightSheer Duet HS handpiece