Clinical trials: Hair Removal
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
Unwanted Fine Facial Hair
Clinical Evaluation to Assess the Safety and Efficacy of GentleMax Pro™/GentleMax Pro Plus™
This clinical study is intended to evaluate the safety and efficacy of the GentleMax Pro Plus™ laser system for its intended use of hair removal while using short pulse durations to improve the efficacy of achieving permanent…
- Trial name
- NCT04975243
- Testing
- GentleMax Pro Plus 755nm and 1064nm laser system
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Candela Corporation
Epilation
Safety and Efficacy of Using LEORTEC-300 System For Hair Removal Treatment
Removal of unwanted hair is one of the most commonly sought cosmetic solutions. Traditional methods, such as shaving, depilatories, tweezing and waxing result in only temporary hair removal, and thus require extensive…
- Trial name
- NCT00348257
- Testing
- Hair removal by laser/IPL device
- Where
- Israel
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Leortec Medical Systems Ltd
Hair Remval
Clinical Evaluation of Splendor X for Hair Removal
At least 40 healthy male or female subjects that wish to remove their hair will be enrolled to this study. Each subject will receive five treatments at 6-8 weeks intervals.
- Trial name
- NCT04152707
- Testing
- Splendor X
- Where
- 2 sites in United States
- Volunteers
- 44 people, healthy volunteers welcome
- Sponsor
- Lumenis Be Ltd.
Wounds and Injuries
Comparison of a Novel Wound Dressing Stratamed Versus Current Clinical Practice After Follicular Unit Extraction Hair Transplantation
Follicular donor sites on the scalp for hair transplantation will be treated with studied products post harvest. A randomized side of the scalp will be treated with Stratamed, the other side with standard clinical practice.
- Trial name
- NCT03843996
- Testing
- Treatment - Stratamed
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Stratpharma AG
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
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.
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.
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
Hirsutism
Clinical Evaluation of Silk'n Glide for Face
This is a clinical study to determine the efficacy and safety of the Glide, hair removal photo-depilation device, for removing facial hairs.
- Trial name
- NCT02103608
- Testing
- Glide
- Volunteers
- 17 people, healthy volunteers welcome
- Sponsor
- Home Skinovations Ltd.
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
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.
Hypertrichosis
A Prospective Multi-Center Study of a Novel Dual-Wavelength Laser for Hair Removal
To evaluate the safety and efficacy of the Cutera excel HR dual wavelength 755nm Alexandrite and 1064nm Nd:YAG laser for hair removal.
- Trial name
- NCT02536092
- Testing
- 755nm and 1064nm Nd:YAG laser
- Where
- 2 sites in Canada
- Volunteers
- healthy volunteers welcome
- Sponsor
- Cutera Inc.
Hypertrichosis
Pilot Study of a Novel IPL for Removal of Unwanted Fine Body Hair
The purpose of this randomized, controlled, open-label pilot study is to evaluate the safety and efficacy of a novel intense pulsed light (IPL) device for removal of unwanted fine body hair.
- Trial name
- NCT01912950
- Testing
- Prowave LX IPL
- Where
- United States
- Volunteers
- 11 people, healthy volunteers welcome
- Sponsor
- Cutera Inc.
Skin Recovery
A Study to Gain Information How Well Dexpanthenol Dermal Spray Helps the Skin to Recover After Laser Hair Removal in the Groin and Intimate Area
In this study, researchers want to learn more about the effect of dexpanthenol dermal spray on skin recovery after a dermatological procedure for hair removal (laser depilation) in the groin and intimate area in adult women.
- Trial name
- NCT03853525
- Testing
- BAY207543 (Bepanthol, Bepantol® Derma Spray), Semisolid vaseline
- Where
- Brazil
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Bayer
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.
Hirsutism, Hypertrichosis
Enhanced Safety Laser Hair Removal System
The purpose of this study is to determine whether a new laser system provides better safety and efficacy in hair removal than existing lasers.
- Trial name
- NCT00441948
- Testing
- Peterio
- Where
- Israel
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Scilex Ltd.
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.
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