Trials / Completed
CompletedNCT01348789
Safety for Frequent Use Conditions of Hair Removal Device
Safety of Hair2Go Device in Frequent Use Conditions: A Prospective, Open Label Study With Before-After Design
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 37 (actual)
- Sponsor
- Syneron Medical · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
To measure the safety of hair removal device when used frequently.
Detailed description
The primary endpoint of this study is to measure the safety of the Hair2Go device when used frequently. The secondary endpoints include the kinetics of the hair clearance up to 8 weeks after the last treatment, and gathering information about the pain associated with the procedure
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Hair2Go (Mē) | Treatment with Hair2Go (Mē) three times every 2-4 days |
Timeline
- Start date
- 2011-03-01
- Primary completion
- 2012-06-01
- Completion
- 2012-06-01
- First posted
- 2011-05-05
- Last updated
- 2013-02-18
- Results posted
- 2013-02-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01348789. Inclusion in this directory is not an endorsement.