Hair Removal Clinical Trial
Official title:
The Efficiency of the Hair2Go Device: A Prospective, Open, Label Study With Before-After Design
The purpose of this study is to determine efficiency of Hair2Go device for short-term and long-term removal of unwanted hair adjunctive to shaving using a before-after study design.
This study is a multicenter study, designed to determine the efficacy of the Hair2Go hair removal device and to compare the extent of hair removal with and without maintenance treatments. Preferably, two anatomical regions to be treated will be selected including the axilla and either the legs (calves) or forearms. The size of the area treated will be approximately 5x5 cm2. Additional areas including the face can be treated according to the subject's request with the PI's discretion but are not mandatory. Subjects will be provided with the device and will be instructed as to the method of usage. The subjects will be expected to self-administer the treatment at the clinic in a "simulated home environment". The duration of the treatment session is approximately 30-60 minutes. Each of the selected anatomical regions (both left and right sides) will be treated with either low, medium, or high Elōs energy level according to the PI's discretion. However all anatomical regions except for the axilla will be treated with either low or medium elōs energy levels only. Only the axilla will be treated up to an energy of 4J//cm2 A defined area of 5x5 cm2cm2 in the leg will not be treated and will serve as a reference for the temporal changes in hair growth that might be subject to factors, including fluctuations in hormone levels. Both sides (left and right) of the same anatomical region will receive the basic treatments. One side will receive 3 additional maintenance treatments in 4 week intervals ("Maintenance" vs "No maintenance" side) until the end of the experiment. More specifically, the study includes up to 11 visits at the clinic: initial consultation, 7 basic treatments in 1 week intervals followed in one side by 3 maintenance treatments, each 4 weeks apart. Follow ups will be conducted at 4 and 12 weeks after the last basic treatment. ;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT00366964 -
The Efficacy Of The Wavelight Mydon Laser for Hair Removal And Treatment of Leg Veins
|
N/A | |
| Completed |
NCT04807205 -
Post Market Study Using The Elite IQ Device
|
N/A | |
| Completed |
NCT01578187 -
Hair2Go Label Comprehension and Usability Study
|
N/A | |
| Completed |
NCT01348789 -
Safety for Frequent Use Conditions of Hair Removal Device
|
N/A | |
| Completed |
NCT01057134 -
Ultrasound Device for Hair Removal
|
||
| Completed |
NCT01282866 -
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
|
N/A | |
| Not yet recruiting |
NCT06179186 -
Hair Removal: Intense Pulsed Light Versus Diode Laser
|
N/A | |
| Completed |
NCT01529931 -
Long Term Efficiency of the Hair2Go Device
|
N/A | |
| Completed |
NCT01801202 -
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
|
N/A | |
| Terminated |
NCT02912013 -
The Efficacy of the Me Mini Device for Hair Removal
|
N/A | |
| Active, not recruiting |
NCT02318654 -
Ice Versus EMLA for Pain in Laser Hair Removal
|
N/A | |
| Completed |
NCT03438929 -
Evaluation of Diolaze XL Blended Mode for Hair Removal
|
N/A | |
| Completed |
NCT03945383 -
Clinical Investigation of Safety and Effectiveness of Emerald IPLdevice
|
N/A | |
| Completed |
NCT03921814 -
Sunstone IPL (Intense Pulsed Light) for Hair Reduction
|
N/A |