Trials / Completed
CompletedNCT01801202
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 21 (actual)
- Sponsor
- Lumenis Be Ltd. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
* The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction. * Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site. * Each subject will receive five treatments at four to six week intervals and return for follow-up visits at three and six months after the last treatment for evaluation of the treated areas.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LightSheer Duet HS handpiece | The approach to be studied here relies on a cleared modality, the LightSheer Duet High Speed (HS) that uses 805 nm diode laser with vacuum (K053628). |
Timeline
- Start date
- 2013-02-01
- Primary completion
- 2014-11-01
- Completion
- 2014-11-01
- First posted
- 2013-02-28
- Last updated
- 2015-04-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01801202. Inclusion in this directory is not an endorsement.