Trials / Completed
CompletedNCT02098811
Evaluation of the Safety and Precursors of Efficacy
Evaluation of the Safety and Efficacy of a Non-Invasive Disruption of Fat and Skin Tightening Using 1064nm and 940nm Wavelengths
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Cynosure, Inc. · Industry
- Sex
- All
- Age
- 20 Years – 55 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate and compare the safety and pre-cursors of efficacy of a non-invasive 1064nm laser and 940nm diode, for the disruption of subcutaneous adipose tissue and skin tightening.
Detailed description
The purpose of the biopsies is to assess if the device causes an inflammatory response in the abdominoplasty tissue that will be excised.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | 1064nm Laser | Patient will be treated with 1064nm Laser prior to abdominoplasty |
| DEVICE | 940nm Laser | Patient will be treated with 940nm Laser prior to abdominoplasty |
Timeline
- Start date
- 2013-06-01
- Primary completion
- 2014-05-01
- Completion
- 2014-05-01
- First posted
- 2014-03-28
- Last updated
- 2020-10-27
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02098811. Inclusion in this directory is not an endorsement.