Clinical trials: Hair Removal
Hair Removal
Ice Versus EMLA for Pain in Laser Hair Removal
The primary objective of this study is to compare the efficacy of ice pack to topical eutectic mixture of local anesthesia (EMLA) for pain control in diode 810 nm laser axillary hair removal.
- Trial name
- NCT02318654
- Testing
- Ice Pack, Topical EMLA cream
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Northwestern University
Hair Reduction, Tattoo Removal
Clinical Study to Evaluate the Safety and Efficacy of Candela Technology
This is a non-randomized, multi-center, open-label, prospective clinical study evaluating the clinical treatment with Candela Medical Technology.
- Conditions
- Hair Reduction, Tattoo Removal, Wrinkle, Acne
- Trial name
- NCT06202274
- Testing
- Nordlys, Gentle, Picoway, Vbeam, Profound, Profound Matrix, eTwo, Exceed, CO2RE
- Where
- 3 sites in United States, Israel
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- Candela Corporation
Hair Removal
Ultrasound Device for Hair Removal
The purpose of this study is to evaluate the safety and efficacy of the Cutera UHAIR ultrasound device for hair removal.
- Trial name
- NCT01057134
- Testing
- Cutera Ultrasound Device
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Cutera Inc.
Hair Removal
Sunstone IPL (Intense Pulsed Light) for Hair Reduction
This is a prospective, multi-center, single-arm, single blinded study to evaluate the safety and efficacy of the Sunstone IPL (Intense Pulsed Light) device to remove hair.
- Trial name
- NCT03921814
- Testing
- Treatment with IPL device
- Where
- 2 sites in United States
- Volunteers
- 102 people, healthy volunteers welcome
- Sponsor
- Philips Healthcare
Hair Removal
Clinical Investigation of Safety and Effectiveness of Emerald IPLdevice
Prospective, multi-center, single-arm, single blinded (Philips hair counter) study in healthy women of skin types I up to and including V.
- Trial name
- Emerald (NCT03945383)
- Testing
- Treatment with IPL device
- Where
- 3 sites in United States
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Philips Healthcare
Hair Removal Treatment
The Trio Laser Module for Hair Removal Treatment
The study is aimed to assess the safety and efficacy of hair removal treatments, using the Trio Laser Module (Alma Lasers). The study will include 36 subjects that will undergo axilla and bikini line hair removal treatments.
- Trial name
- NCT04599751
- Testing
- Hair removal treatment
- Where
- 2 sites in United States
- Volunteers
- 37 people, healthy volunteers welcome
- Sponsor
- Alma Lasers
Removal of Excess or Unwanted Body Hair
Clinical Evaluation of Hair Removal and Permanent Hair Reduction for Skin Types VI Using Intense Pulsed Light
This is a Multi-center, blinded, baseline-controlled, prospective study to evaluate permanent hair reduction and removal for skin types V and VI using IPL.
- Trial name
- NCT02452398
- Testing
- Treatment group, No intervention
- Where
- United States
- Volunteers
- 79 people, healthy volunteers welcome
- Sponsor
- Venus Concept
Hair Removal
Long Term Efficiency of the Hair2Go Device
The current study is a follow up study designed to gather information about the effect of the number of Hair2Go maintenance treatments on hair clearance 1 year after the last basic Hair2Go treatment.
- Trial name
- OHR-8-FU-1Y (NCT01529931)
- Testing
- Hair2Go
- Where
- 3 sites in United States
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Hair Removal
Evaluation of Diolaze XL Blended Mode for Hair Removal
The objective of this clinical study is to evaluate safety and efficiency of Diolase XL blended modes for hair removal. The handpieces tested were a blend of 755nm/810nm and 810nm/1064nm.
- Trial name
- NCT03438929
- Testing
- Diode laser
- Where
- Israel
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- InMode MD Ltd.
Hair Removal
The Efficacy of the Me Mini Device for Hair Removal
The Mē Mini is a compact version of the Mē device that was cleared by the FDA for removal of unwanted hair and for permanent hair reduction for all skin colors (Fitzpatrick skin photo-types I-VI) based on a series of multi-site…
- Trial name
- OHR2-MeMini (NCT02912013)
- Testing
- Me Mini
- Where
- Israel
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Iluminage Ltd.
Hair Removal
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
The objective of this clinical study is to verify hair count reduction, associated comfort/discomfort and treatment time using the LightSheer Duet System with the High Speed (HS) handpieces for temporary hair removal and…
- Trial name
- NCT01282866
- Testing
- LightSheer Duet
- Where
- United States
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Lumenis Be Ltd.
Laser Hair Removal in Healthy Subjects
The Effect of Laser Hair Removal on Permanent Hair Reduction
The purpose of this study is to learn more about how hair removal with lasers achieves, what appears to be, permanent hair reduction.
- Trial name
- NCT00279643
- Testing
- Laser Hair Removal
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- University of Michigan
Hair Removal
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
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.
- Trial name
- NCT01801202
- Testing
- LightSheer Duet HS handpiece
- Where
- United States
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- Lumenis Be Ltd.
Leg Veins, Hair Removal
The Efficacy Of The Wavelight Mydon Laser for Hair Removal And Treatment of Leg Veins
This study is being done to compare the efficacy of an FDA cleared laser device with other similar systems in the market for the treatment of leg veins and hair removal in patients with darker skin type.
- Trial name
- NCT00366964
- Testing
- Laser Treatment, Wave Light laser device for skin treatment
- Where
- United States
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- University of California, Davis
Hair Removal
Hair2Go Label Comprehension and Usability Study
The purpose of this study is to test label comprehension and usability of the hair removal device in 60 male and female participants.
- Trial name
- OHR6-LCU (NCT01578187)
- Testing
- Hair2Go
- Where
- United States
- Volunteers
- 63 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Hair Removal
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.
- Trial name
- NCT01348776
- Testing
- Hair2Go (Mē)
- Where
- 4 sites in United States
- Volunteers
- 87 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Hair Removal
Safety for Frequent Use Conditions of Hair Removal Device
To measure the safety of hair removal device when used frequently.
- Trial name
- OHR-3 (NCT01348789)
- Testing
- Hair2Go (Mē)
- Where
- United States
- Volunteers
- 37 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Laser Hair Removal
Evaluation of the LightSheer HS Hand Piece as Compared to the LightSheer ET Hand Piece for the Intended Use of Hair Removal and Permanent Hair Reduction
To observe the qualitative comparison of follicular damage between treatment with the LightSheer Duet hand pieces (ET and HS) as assessed by horizontal biopsy.
- Trial name
- NCT00657085
- Where
- United States
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Lumenis Be Ltd.