At a glance
ClinicalIndex Comparison RecordN/ACompleted· 22 enrolled
Drug / intervention
1064 nm Nd:YAG laserdevice
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.
Evaluation of the Candela 1064nm:Nd:YAG Laser for Skin Tightening
In Brief
A clinical study evaluating 1064 nm Nd:YAG laser for Localized Lipodystrophy. Completed, enrolled 22 participants across 2 sites.
Detailed Summary
The purpose of this research study is to evaluate effectiveness of a non-ablative (does not remove skin) treatment for cellulite (dimpled fat) in conjunction with skin tightening using the Candela GentleYAG laser.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLocalized Lipodystrophy
CountriesUnited States
CollaboratorsCandela Corporation
Timeline
N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartOct 2006
First PostedJan 2008
Primary CompletionDec 2009
Study CompletionJan 2010
TodayJul 2026
First PostedJan 3, 2008
Enrollment StartOct 1, 2006
Primary CompletionDec 1, 2009
Study CompletionJan 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 18.5 years ago
Interventions
1064 nm Nd:YAG laserdevice
3 treatments at 3-5 week intervals Spot size: 10 - 18 mm diameter Fluence: 50 J/cm2 Laser pulse duration: 50 ms Rep. rate: Up to 2 Hz DCD cooling 0-50 ms